M. Krische

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Dynamic Combinatorial Chemistry: Substrate H-Bonding Directed Assembly of Receptors Based on Bipyridine-Metal Complexes

J. Lehn, I. Huc, M. Krische, 1999 .

Catalytic diastereoselective synthesis of diquinanes from acyclic precursors.

M. Krische, Jian-Cheng Wang, Sze-Sze Ng, 2003, Journal of the American Chemical Society.

Asymmetric total synthesis of the iridoid beta-glucoside (+)-geniposide via phosphine organocatalysis.

M. Krische, R. Jones, 2009, Organic letters.

Synthesis of seco-B-Ring Bryostatin Analogue WN-1 via C–C Bond-Forming Hydrogenation: Critical Contribution of the B-Ring in Determining Bryostatin-like and Phorbol 12-Myristate 13-Acetate-like Properties

Megan L. Peach, P. Blumberg, M. Peach, 2014, Journal of the American Chemical Society.

Direct generation of acyclic polypropionate stereopolyads via double diastereo- and enantioselective iridium-catalyzed crotylation of 1,3-diols: beyond stepwise carbonyl addition in polyketide construction.

M. Krische, Xin Gao, Hoon Han, 2011, Journal of the American Chemical Society.

Diastereo- and enantioselective ruthenium-catalyzed hydrohydroxyalkylation of 2-silyl-butadienes: carbonyl syn-crotylation from the alcohol oxidation level.

M. Krische, J. Zbieg, J. Moran, 2011, Journal of the American Chemical Society.

Total synthesis of (+)-roxaticin via C-C bond forming transfer hydrogenation: a departure from stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles in polyketide construction.

M. Krische, S. Han, Abbas Hassan, 2010, Journal of the American Chemical Society.

1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols.

M. Krische, Abbas Hassan, I. Kim, 2009, Angewandte Chemie.

Total Synthesis of the Acetyl CoA Carboxylase Inhibitor Soraphen A: Asymmetric Tsuji Reduction Enables Successive Olefin Metathesis.

M. Krische, Tabitha T. Schempp, Tabitha T Schempp, 2022, Journal of the American Chemical Society.

4.6 C–C Bond Formation (Metal-Catalyzed Reductive Aldol Coupling)

Hye‐Young Jang, M. Krische, 2012 .

Anion radical chain cycloaddition of tethered enones: intramolecular cyclobutanation and Diels-Alder cycloaddition.

V. Lynch, Hye‐Young Jang, Yeonsuk Roh, 2002, Organic letters.

Chemically induced anion radical cycloadditions: intramolecular cyclobutanation of bis(enones) via homogeneous electron transfer.

M. Krische, Greg A N Felton, N. L. Bauld, 2004, Journal of the American Chemical Society.

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level using allyl acetate as an allyl metal surrogate.

M. Krische, I. Kim, Ming‐Yu Ngai, 2008, Journal of the American Chemical Society.

Evaluation of Chromane-Based Bryostatin Analogues Prepared via Hydrogen-Mediated C-C Bond Formation: Potency Does Not Confer Bryostatin-like Biology.

P. Blumberg, M. Krische, N. Lewin, 2016, Journal of the American Chemical Society.

Total synthesis of bryostatin 7 via C-C bond-forming hydrogenation.

M. Krische, Yu Lu, S. Woo, 2011, Journal of the American Chemical Society.

Redox-Triggered C–C Coupling of Alcohols and Vinyl Epoxides: Diastereo- and Enantioselective Formation of All-Carbon Quaternary Centers via tert-(Hydroxy)-Prenylation

Jiajie Feng, M. Krische, Victoria J. Garza, 2014, Journal of the American Chemical Society.

Enantioselective Ruthenium-Catalyzed Benzocyclobutenone-Ketol Cycloaddition: Merging C-C Bond Activation and Transfer Hydrogenative Coupling for Type II Polyketide Construction.

Ben W. H. Turnbull, M. Krische, Brett R. Ambler, 2018, Journal of the American Chemical Society.

Enantioselective Iridium-Catalyzed Phthalide Formation through Internal Redox Allylation of Phthalaldehydes.

M. Krische, James M. Cabrera, J. Tauber, 2018, Angewandte Chemie.

Chemo-, regio-, and enantioselective Pd-catalyzed allylic alkylation of indolocarbazole pro-aglycons.

B. Trost, V. Berl, M. Krische, 2002, Organic letters.

Mechanism and origins of regio- and enantioselectivities in RhI-catalyzed hydrogenative couplings of 1,3-diynes and activated carbonyl partners: intervention of a cumulene intermediate.

K. Houk, Peng Liu, M. Krische, 2011, Chemistry.

Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level.

M. Krische, F. Shibahara, 2008, Chemistry letters.

Metal-catalyzed Reductive Carbocyclization (C C, C C, C O Bonds)

Hye‐Young Jang, M. Krische, 2007 .

Ruthenium-catalyzed C-C coupling of fluorinated alcohols with allenes: dehydrogenation at the energetic limit of β-hydride elimination.

M. Krische, Brannon Sam, Tom Luong, 2015, Angewandte Chemie.

Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological Space

Jared T. Shaw, Derek S. Tan, D. E. Olson, 2018, ACS central science.

Enantioselective Total Synthesis of Andrographolide and 14-Hydroxy-Colladonin: Carbonyl Reductive Coupling and trans-Decalin Formation via Hydrogen Transfer.

M. Krische, T. Wurm, Lin Yang, 2020, Angewandte Chemie.

Enantioselective Total Synthesis of Andrographolide and 14‐Hydroxy‐Colladonin: Carbonyl Reductive Coupling and trans ‐Decalin Formation by Hydrogen Transfer

M. Krische, T. Wurm, Lin Yang, 2020, Angewandte Chemie.

Total Synthesis of Leiodermatolide A via Transfer Hydrogenative Allylation, Crotylation, and Propargylation: Polyketide Construction beyond Discrete Allyl- or Allenylmetal Reagents.

M. Krische, Y. Siu, J. Roane, 2021, Journal of the American Chemical Society.

Synthesis of the C(1)–C(13) Fragment of Leiodermatolide via Hydrogen-Mediated C–C Bond Formation

M. Krische, S. D. Ramgren, J. Roane, 2017, Organic letters.

Total Synthesis of Swinholide A: An Exposition in Hydrogen-Mediated C-C Bond Formation.

M. Krische, Suckchang Hong, I. Shin, 2016, Journal of the American Chemical Society.

Formal Synthesis of Premisakinolide A and C(19)-C(32) of Swinholide A via Site-Selective C-H Allylation and Crotylation of Unprotected Diols.

M. Krische, I. Shin, 2015, Organic letters.

Ruthenium-Catalyzed Asymmetric Hydrohydroxyalkylation of Butadiene: The Role of the Formyl Hydrogen Bond in Stereochemical Control.

Matthew N. Grayson, K. Houk, M. Krische, 2015, Journal of the American Chemical Society.

Ruthenium catalyzed reductive coupling of paraformaldehyde to trifluoromethyl allenes: CF3-bearing all-carbon quaternary centers.

M. Krische, T. Montgomery, Brannon Sam, 2013, Organic letters.

Consecutive iridium catalyzed C-C and C-H bond forming hydrogenations for the diastereo- and enantioselective synthesis of syn-3-fluoro-1-alcohols: C-H (2-fluoro)allylation of primary alcohols.

M. Krische, Abbas Hassan, T. Montgomery, 2012, Chemical communications.

Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (α-trifluoromethyl)allylation from the alcohol or aldehyde oxidation level.

M. Krische, Xin Gao, Yong Jian Zhang, 2011, Angewandte Chemie.

Benzannulation via Ruthenium(0)-Catalyzed Transfer Hydrogenative Cycloaddition: Precision Synthesis and Photophysical Characterization of Soluble Diindenoperylenes.

S. Roberts, M. Krische, J. A. Bender, 2020, Chemistry.

Benzannulation via ruthenium-catalyzed diol-diene [4+2] cycloaddition: one- and two-directional syntheses of fluoranthenes and acenes.

M. Krische, Laina M. Geary, T. Montgomery, 2014, Journal of the American Chemical Society.

Synthetic duplex oligomers: optimizing interstrand affinity through the use of a noncovalent constraint

V. Lynch, M. Krische, E. A. Archer, 2002 .

Enantioselective total and formal syntheses of paroxetine (PAXIL) via phosphine-catalyzed enone α-arylation using arylbismuth(V) reagents: a regiochemical complement to Heck arylation

Phillip K. Koech, M. Krische, 2006 .

Chiral α-Stereogenic Oxetanols and Azetidinols via Alcohol-Mediated Reductive Coupling of Allylic Acetates: Enantiotopic π-Facial Selection in Symmetric Ketone Addition.

M. Krische, Nicholas P. Stafford, Melinda J. Cheng, 2022, ACS catalysis.

Alkynes as Electrophilic or Nucleophilic Allylmetal Precursors in Transition-Metal Catalysis.

M. Krische, B. Breit, Alexander M. Haydl, 2017, Angewandte Chemie.

Ruthenium(0)-Catalyzed C-C Coupling of Alkynes and 3-Hydroxy-2-oxindoles: Direct C-H Vinylation of Alcohols.

K. Qu, M. Krische, Shujie Chen, 2017, Organic letters.

Fluorous Chemistry

C. Hunter, K. Houk, R. Naaman, 2012 .

Enantioselective Metal-Catalyzed Reductive Coupling of Alkynes with Carbonyl Compounds and Imines: Convergent Construction of Allylic Alcohols and Amines.

Yu-Hsiang Chang, M. Krische, Jon Shezaf, 2022, ACS catalysis.

Organometallics Roundtable 2013–2014

Patrick L. Holland, C. E. Webster, Connie C. Lu, 2014 .

Ruthenium(0)-Catalyzed Cycloaddition of 1,2-Diols, Ketols, or Diones via Alcohol-Mediated Hydrogen Transfer.

Ben W. H. Turnbull, K. Fukaya, M. Krische, 2018, Angewandte Chemie.

Fracture Between Self-Assembled Monolayers

K. Liechti, M. Krische, S. R. Na, 2009 .

Formation of C-C Bonds via Iridium-Catalyzed Hydrogenation and Transfer Hydrogenation.

M. Krische, J. Bower, J. F. Bower, 2011, Topics in organometallic chemistry.

First catalytic reductive coupling of 1,3-diynes to carbonyl partners: a new regio- and enantioselective C-C bond forming hydrogenation.

Hye‐Young Jang, M. Krische, Ryan R. Huddleston, 2003, Journal of the American Chemical Society.

Stereo- and Site-Selective Conversion of Primary Alcohols to Allylic Alcohols via Ruthenium-Catalyzed Hydrogen Auto-Transfer Mediated by 2-Butyne.

M. Krische, Jon Shezaf, Eliezer Ortiz, 2022, Journal of the American Chemical Society.

Diastereo- and Enantioselective Ruthenium-Catalyzed C-C Coupling of 1-Arylpropynes and Alcohols: Alkynes as Chiral Allylmetal Precursors in Carbonyl anti-(α-Aryl)allylation.

M. Krische, M. Xiang, Ankan Ghosh, 2021, Journal of the American Chemical Society.

Intermolecular Metal-Catalyzed Reductive Coupling of Dienes, Allenes, and Enynes with Carbonyl Compounds and Imines.

M. Krische, Michael R. Holmes, Leyah A. Schwartz, 2018, Chemical reviews.

Catalytic Reductive Aldol and Mannich Reactions of Enone, Acrylate, and Vinyl Heteroaromatic Pronucleophiles.

M. Krische, Eliezer Ortiz, Cole C. Meyer, 2020, Chemical reviews.

Unlocking Hydrogenation for C-C Bond Formation: A Brief Overview of Enantioselective Methods.

M. Krische, Abbas Hassan, 2011, Organic process research & development.

Catalytic Reductive Coupling of Alkenes and Alkynes to Carbonyl Compounds and Imines Mediated by Hydrogen

M. Krische, Hiroki Iida, 2007 .

Enolate generation under hydrogenation conditions: catalytic aldol cycloreduction of keto-enones.

M. Krische, Ryan R. Huddleston, 2003, Organic letters.

Enantioselective Formation of All-Carbon Quaternary Centers via C-H Functionalization of Methanol: Iridium-Catalyzed Diene Hydrohydroxymethylation.

M. Krische, D. Herkommer, K. D. Nguyen, 2016, Journal of the American Chemical Society.

Osmium(0)-Catalyzed C-C Coupling of Ethylene and α-Olefins with Diols, Ketols, or Hydroxy Esters via Transfer Hydrogenation.

M. Krische, Boyoung Y. Park, Tom Luong, 2016, The Journal of organic chemistry.

Branch-selective intermolecular hydroacylation: hydrogen-mediated coupling of anhydrides to styrenes and activated olefins.

Young‐Taek Hong, M. Krische, A. Barchuk, 2006, Angewandte Chemie.

Allenes and Dienes as Chiral Allylmetal Pronucleophiles in Catalytic Enantioselective C=X Addition: Historical Perspective and State-of-The-Art Survey.

M. Krische, M. Xiang, Dana E Pfaffinger, 2021, Chemistry.

Triple Helical Ir(ppy)3 Phenylene Cage Prepared by Diol-Mediated Benzannulation: Synthesis, Resolution, Absolute Stereochemistry and Photophysical Properties.

D. Armstrong, S. Roberts, M. Krische, 2019, Chemistry.

Alkynes as synthetic equivalents to stabilized Wittig reagents: intra- and intermolecular carbonyl olefinations catalyzed by Ag(I), BF3, and HBF4.

M. Krische, J. Rhee, 2005, Organic letters.

Transition Metal Catalyzed Cycloisomerizations

B. Trost, M. Krische, 1998 .

Chemical Tuning of Exciton versus Charge-Transfer Excited States in Conformationally Restricted Arylene Cages.

C. Bardeen, D. Casanova, M. Krische, 2021, Journal of the American Chemical Society.

Regio‐ and Stereoselective Construction of γ‐Butenolides Through Phosphine‐Catalyzed Substitution of Morita—Baylis—Hillman Acetates: An Organocatalytic Allylic Alkylation.

M. Krische, C. Cho, 2005 .

Phosphine‐Catalyzed Regiospecific Allylic Amination and Dynamic Kinetic Resolution of Morita—Baylis—Hillman Acetates.

M. Krische, J. Kong, C. Cho, 2004 .

Iridium-, Ruthenium-, and Nickel-Catalyzed C-C Couplings of Methanol, Formaldehyde, and Ethanol with π-Unsaturated Pronucleophiles via Hydrogen Transfer.

M. Krische, Cole C. Meyer, 2022, The Journal of organic chemistry.

Application of a high-throughput enantiomeric excess optical assay involving a dynamic covalent assembly: parallel asymmetric allylation and ee sensing of homoallylic alcohols

H. Jo, E. Anslyn, M. Krische, 2015, Chemical science.

Direct C-C Coupling of Ethylene and α -Olefins with Diols, Ketols or Hydroxy Esters via Osmium(0) Catalyzed Transfer Hydrogenation

Hiroki Sato, M. Krische, Boyoung Y. Park, 2016 .

Catalytic carbonyl Z-dienylation via multicomponent reductive coupling of acetylene to aldehydes and alpha-ketoesters mediated by hydrogen: Carbonyl insertion into cationic rhodacyclopentadienes.

M. Krische, J. Kong, 2006, Journal of the American Chemical Society.

Enantioselective reductive coupling of alkynes and alpha-keto aldehydes via rhodium-catalyzed hydrogenation: an approach to bryostatin substructures.

M. Krische, C. Cho, 2006, Organic letters.

Enantiomerically enriched allylic alcohols and allylic amines via C-C bond-forming hydrogenation: asymmetric carbonyl and imine vinylation.

M. Krische, Ming‐Yu Ngai, V. Komanduri, 2007, Accounts of chemical research.

Total Synthesis of Cryptocaryol A by Enantioselective Iridium-Catalyzed Alcohol C-H Allylation.

M. Krische, A. Waldeck, F. Perez, 2016, Angewandte Chemie.

Selection between Diastereomeric Kinetic vs Thermodynamic Carbonyl Binding Modes Enables Enantioselective Iridium-Catalyzed anti-(α-Aryl)allylation of Aqueous Fluoral Hydrate and Difluoroacetaldehyde Ethyl Hemiacetal.

M. Krische, M. Xiang, James M. Cabrera, 2018, Journal of the American Chemical Society.

Iridium-catalyzed allylation of chiral β-stereogenic alcohols: bypassing discrete formation of epimerizable aldehydes.

M. Krische, Daniel C. Schmitt, Anne-Marie R. Dechert-Schmitt, 2012, Organic letters.

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol oxidation level via transfer hydrogenation: minimizing pre-activation for synthetic efficiency.

M. Krische, S. Han, I. Kim, 2009, Chemical communications.

Enantioselective allylation, crotylation, and reverse prenylation of substituted isatins: iridium-catalyzed C-C bond-forming transfer hydrogenation.

M. Krische, J. Itoh, S. Han, 2009, Angewandte Chemie.

Concise synthesis of the bryostatin A-ring via consecutive C-C bond forming transfer hydrogenations.

M. Krische, Yu Lu, 2009, Organic letters.

Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.

Jiajie Feng, M. Krische, Michael R. Holmes, 2017, Chemical reviews.

Ruthenium(0)-Catalyzed [4+2] Cycloaddition of Acetylenic Aldehydes with α-Ketols: Convergent Construction of Angucycline Ring Systems.

M. Krische, A. Saxena, F. Perez, 2016, Angewandte Chemie.

Feedstock Reagents in Metal-Catalyzed Carbonyl Reductive Coupling: Minimizing Preactivation for Efficiency in Target-Oriented Synthesis.

Rosalie S. Doerksen, M. Krische, Rosalie S Doerksen, 2019, Angewandte Chemie.

Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.

Jiajie Feng, M. Krische, Zachary A. Kasun, 2016, Journal of the American Chemical Society.

Catalyst-directed diastereo- and site-selectivity in successive nucleophilic and electrophilic allylations of chiral 1,3-diols: protecting-group-free synthesis of substituted pyrans.

M. Krische, Gang‐Wei Wang, I. Shin, 2014, Chemistry.

Catalytic enantioselective C-H functionalization of alcohols by redox-triggered carbonyl addition: borrowing hydrogen, returning carbon.

M. Krische, John M. Ketcham, T. Montgomery, 2014, Angewandte Chemie.

Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition.

M. Krische, T. Itoh, Daniel C. Schmitt, 2014, Natural product reports.

Total synthesis of cyanolide A in the absence of protecting groups, chiral auxiliaries, or premetalated carbon nucleophiles.

M. Krische, A. Waldeck, 2013, Angewandte Chemie.

Protecting-group-free diastereoselective C-C coupling of 1,3-glycols and allyl acetate through site-selective primary alcohol dehydrogenation.

M. Krische, Daniel C. Schmitt, Anne-Marie R. Dechert-Schmitt, 2013, Angewandte Chemie.

Chiral-anion-dependent inversion of diastereo- and enantioselectivity in carbonyl crotylation via ruthenium-catalyzed butadiene hydrohydroxyalkylation.

M. Krische, E. Yamaguchi, E. McInturff, 2012, Journal of the American Chemical Society.

Enantioselective C-H Crotylation of Primary Alcohols via Hydrohydroxyalkylation of Butadiene

M. Krische, J. Zbieg, E. Yamaguchi, 2012, Science.

Enhanced anti-diastereo- and enantioselectivity in alcohol-mediated carbonyl crotylation using an isolable single component iridium catalyst.

M. Krische, Xin Gao, I. Townsend, 2011, The Journal of organic chemistry.

anti-Diastereo- and enantioselective carbonyl crotylation from the alcohol or aldehyde oxidation level employing a cyclometallated iridium catalyst: alpha-methyl allyl acetate as a surrogate to preformed crotylmetal reagents.

M. Krische, S. Han, I. Kim, 2009, Journal of the American Chemical Society.

Enantioselective iridium-catalyzed carbonyl allylation from the alcohol or aldehyde oxidation level via transfer hydrogenative coupling of allyl acetate: departure from chirally modified allyl metal reagents in carbonyl addition.

Michael J. Krische, In Su Kim, M. Krische, 2008, Journal of the American Chemical Society.

Enantioselective Synthesis of Oxetanes Bearing All-Carbon Quaternary Stereocenters via Iridium-Catalyzed C-C Bond-Forming Transfer Hydrogenation.

M. Krische, Yian Guo, Wonchul Lee, 2017, Chemistry.

Enantioselective iridium-catalyzed vinylogous Reformatsky-aldol reaction from the alcohol oxidation level: linear regioselectivity by way of carbon-bound enolates.

M. Krische, J. Zbieg, Abbas Hassan, 2011, Angewandte Chemie.

Phosphine-mediated reductive condensation of gamma-acyloxy butynoates: a diversity oriented strategy for the construction of substituted furans.

M. Krische, Jian-Cheng Wang, C. Jung, 2004, Journal of the American Chemical Society.

Intramolecular organocatalytic [3+2] dipolar cycloaddition: stereospecific cycloaddition and the total synthesis of (+/-)-hirsutene.

M. Krische, Jian-Cheng Wang, 2003, Angewandte Chemie.

From Hydrogenation to Transfer Hydrogenation to Hydrogen Auto-Transfer in Enantioselective Metal-Catalyzed Carbonyl Reductive Coupling: Past, Present, and Future.

M. Krische, C. G. Santana, 2021, ACS catalysis.

Hydrogen-Mediated C−C Bond Formation: Stereo- and Site-Selective Chemical Synthesis Beyond Stoichiometric Organometallic Reagents

M. Krische, Leyah A. Schwartz, 2018 .

Catalytic Enantioselective Carbonyl Allylation and Propargylation via Alcohol-Mediated Hydrogen Transfer: Merging the Chemistry of Grignard and Sabatier.

S. W. Kim, M. Krische, Wandi Zhang, 2017, Accounts of chemical research.

C-Propargylation Overrides O-Propargylation in Reactions of Propargyl Chloride with Primary Alcohols: Rhodium-Catalyzed Transfer Hydrogenation.

M. Krische, S. Woo, T. Liang, 2016, Angewandte Chemie.

Diastereo- and Enantioselective Iridium Catalyzed Coupling of Vinyl Aziridines with Alcohols: Site-Selective Modification of Unprotected Diols and Synthesis of Substituted Piperidines.

M. Krische, Jana Franke, Gang‐Wei Wang, 2015, Journal of the American Chemical Society.

Formation of C-C BONDS via Catalytic Hydrogenation and Transfer Hydrogenation

M. Krische, J. Moran, 2013 .

Enantioselective conversion of primary alcohols to α-exo-methylene γ-butyrolactones via iridium-catalyzed C-C bond-forming transfer hydrogenation: 2-(alkoxycarbonyl)allylation.

M. Krische, Abbas Hassan, Boyoung Y. Park, 2012, Journal of the American Chemical Society.

Catalytic enantioselective Grignard Nozaki-Hiyama methallylation from the alcohol oxidation level: chloride compensates for π-complex instability.

M. Krische, Abbas Hassan, I. Townsend, 2011, Chemical communications.

Total synthesis of (+)-trienomycins A and F via C-C bond-forming hydrogenation and transfer hydrogenation.

M. Krische, David J Del Valle, 2013, Journal of the American Chemical Society.

Amplification of anti-diastereoselectivity via Curtin-Hammett effects in ruthenium-catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes: diastereoselective formation of all-carbon quaternary centers.

Joyce C. Leung, M. Krische, J. Zbieg, 2011, Journal of the American Chemical Society.

Iridium Catalyzed Hydro-hydroxyalkylation of Butadiene: Carbonyl Crotylation.

M. Krische, J. Zbieg, T. Fukuzumi, 2010, Advanced synthesis & catalysis.

Iridium-catalyzed anti-diastereo- and enantioselective carbonyl (trimethylsilyl)allylation from the alcohol or aldehyde oxidation level.

M. Krische, Xin Gao, S. Han, 2010, Journal of the American Chemical Society.

anti-Diastereo- and enantioselective carbonyl (hydroxymethyl)allylation from the alcohol or aldehyde oxidation level: allyl carbonates as allylmetal surrogates.

M. Krische, Yong Jian Zhang, Sang Hoon Kim, 2010, Journal of the American Chemical Society.

Enantioselective carbonyl allylation, crotylation, and tert-prenylation of furan methanols and furfurals via iridium-catalyzed transfer hydrogenation.

M. Krische, A. Hashmi, Ryan L. Patman, 2010, The Journal of organic chemistry.

Diastereo- and enantioselective anti-alkoxyallylation employing allylic gem-dicarboxylates as allyl donors via iridium-catalyzed transfer hydrogenation.

M. Krische, Hoon Han, S. Han, 2010, Journal of the American Chemical Society.

Elongation of 1,3-polyols via iterative catalyst-directed carbonyl allylation from the alcohol oxidation level.

M. Krische, Abbas Hassan, Yu Lu, 2009, Organic letters.

Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-dimethylallene as the prenyl donor.

M. Krische, Hoon Han, S. Han, 2009, Journal of the American Chemical Society.

Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.

M. Krische, J. Bower, I. Kim, 2009, Angewandte Chemie.

Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition of Carbonyl Compounds and Imines.

M. Krische, I. Kim, J. F. Bower, 2010, Aldrichimica acta.

Formation of C-C Bonds via Ruthenium Catalyzed Transfer Hydrogenation: Carbonyl Addition from the Alcohol or Aldehyde Oxidation Level.

M. Krische, F. Shibahara, 2008, Chemistry letters.

Catalyst-directed diastereoselectivity in hydrogenative couplings of acetylene to alpha-chiral aldehydes: formal synthesis of all eight L-hexoses.

M. Krische, S. Han, J. Kong, 2008, Organic letters.

Hydrogen-mediated C-C bond formation: a broad new concept in catalytic C-C coupling.

M. Krische, Ming‐Yu Ngai, J. Kong, 2007, The Journal of organic chemistry.

Catalytic diastereoselective synthesis of diquinanes from acyclic precursors.

M. Krische, Jian-Cheng Wang, Sze-Sze Ng, 2003, Journal of the American Chemical Society.

Enantioselective Formation of CF3-Bearing All-Carbon Quaternary Stereocenters via C-H Functionalization of Methanol: Iridium Catalyzed Allene Hydrohydroxymethylation.

M. Krische, K. D. Nguyen, Tom Luong, 2017, Journal of the American Chemical Society.

Hydroxymethylation beyond Carbonylation: Enantioselective Iridium-Catalyzed Reductive Coupling of Formaldehyde with Allylic Acetates via Enantiotopic π-Facial Discrimination.

M. Krische, Victoria J. Garza, 2016, Journal of the American Chemical Society.

Iridium-catalysed direct C–C coupling of methanol and allenes

Ryan A. Mesch, M. Krische, J. Moran, 2011, Nature Chemistry.

Iridium-Catalyzed C-C Coupling of a Simple Propargyl Ether with Primary Alcohols: Enantioselective Homoaldol Addition via Redox-Triggered (Z)-Siloxyallylation.

M. Krische, Wandi Zhang, T. Liang, 2015, Journal of the American Chemical Society.

Reductive Cyclization of Halo-Ketones to Form 3-Hydroxy-2-Oxindoles via Palladium Catalyzed Hydrogenation: A Hydrogen-Mediated Grignard Addition.

M. Krische, S. D. Ramgren, I. Shin, 2015, Tetrahedron.

Asymmetric Iridium-Catalyzed C-C Coupling of Chiral Diols via Site-Selective Redox-Triggered Carbonyl Addition.

M. Krische, I. Shin, 2016, Topics in current chemistry.

Iridium-catalyzed C-C coupling via transfer hydrogenation: carbonyl addition from the alcohol or aldehyde oxidation level employing 1,3-cyclohexadiene.

M. Krische, J. F. Bower, Ryan L. Patman, 2008, Organic Letters.

Rhodium-Catalyzed Aldehyde Arylation via Formate-Mediated Transfer Hydrogenation: Beyond Metallic Reductants in Grignard/Nozaki-Hiyami-Kishi-Type Addition.

M. Krische, J. C. Ruble, R. A. Swyka, 2019, Journal of the American Chemical Society.

Diastereoselective cycloreductions and cycloadditions catalyzed by Co(dpm)(2)-silane (dpm = 2,2,6,6-tetramethylheptane-3,5-dionate): mechanism and partitioning of hydrometallative versus anion radical pathways.

V. Lynch, Hye‐Young Jang, Yeonsuk Roh, 2002, Journal of the American Chemical Society.

Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes.

M. Krische, Ming‐Yu Ngai, E. Skucas, 2008, Organic letters.

Hydrogenation for CC Bond Formation

M. Krische, J. Bower, J. F. Bower, 2010 .

Direct Copper-Free Domino Conjugate Addition-Cycloallylation using Organozinc Reagents.

M. Krische, V. Komanduri, Fernando Pedraza, 2008, Advanced synthesis & catalysis.

Desymmetrization of enone-diones via rhodium-catalyzed diastereo- and enantioselective tandem conjugate addition-aldol cyclization.

M. Krische, Longcheng Wang, B. M. Bocknack, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Copper-catalyzed tandem conjugate addition-electrophilic trapping: ketones, esters, and nitriles as terminal electrophiles.

M. Krische, K. Agapiou, David F. Cauble, 2004, Journal of the American Chemical Society.

Paraformaldehyde and methanol as C1 feedstocks in metal-catalyzed C-C couplings of π-unsaturated reactants: beyond hydroformylation.

M. Krische, B. Breit, Brannon Sam, 2015, Angewandte Chemie.

Regiodivergent reductive coupling of 2-substituted dienes to formaldehyde employing ruthenium or nickel catalyst: hydrohydroxymethylation via transfer hydrogenation

M. Krische, Brannon Sam, Alexander Kopfer, 2013 .

Divergent regioselectivity in the synthesis of trisubstituted allylic alcohols by nickel- and ruthenium-catalyzed alkyne hydrohydroxymethylation with formaldehyde.

M. Krische, B. Breit, Cory C. Bausch, 2011, Angewandte Chemie.

Catalytic intermolecular hydroacylation of C–C π-bonds in the absence of chelation assistance

Joyce C. Leung, M. Krische, 2012 .

Enantioselective reductive cyclization of 1,6-enynes via rhodium-catalyzed asymmetric hydrogenation: C-C bond formation precedes hydrogen activation.

J. Brodbelt, Hye‐Young Jang, M. Krische, 2005, Journal of the American Chemical Society.

Diols, α-Ketols, and Diones as 22π Components in [2+2+2] Cycloadditions of 1,6-Diynes via Ruthenium(0)-Catalyzed Transfer Hydrogenation.

M. Krische, Weijie Chen, Hiroki Sato, 2016, Journal of the American Chemical Society.

Rhodium-catalyzed reductive cyclization of 1,6-diynes and 1,6-enynes mediated by hydrogen: catalytic C-C bond formation via capture of hydrogenation intermediates.

Hye‐Young Jang, M. Krische, 2004, Journal of the American Chemical Society.

Catalytic C-C bond formation via capture of hydrogenation intermediates.

Hye‐Young Jang, M. Krische, 2004, Accounts of chemical research.

Hydroacylation of 2-Butyne from the Alcohol or Aldehyde Oxidation Level via Ruthenium Catalyzed C-C Bond Forming Transfer Hydrogenation.

Joyce C. Leung, M. Krische, Vanessa M. Williams, 2009, Tetrahedron.

Direct prenylation of aromatic and alpha,beta-unsaturated carboxamides via iridium-catalyzed C-H oxidative addition-allene insertion.

M. Krische, Yong Jian Zhang, E. Skucas, 2009, Organic letters.

Organocatalytic Michael cycloisomerization of bis(enones): the intramolecular Rauhut-Currier reaction.

Hye‐Young Jang, M. Krische, K. Agapiou, 2002, Journal of the American Chemical Society.

All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation.

T. Smejkal, M. Krische, B. Breit, 2009, Journal of the American Chemical Society.

Diene hydroaminomethylation via ruthenium-catalyzed C–C bond forming transfer hydrogenation: beyond carbonylation

S. Oda, M. Krische, Jana Franke, 2015, Chemical science.

Hydroaminomethylation Beyond Carbonylation: Allene-Imine Reductive Coupling by Ruthenium-Catalyzed Transfer Hydrogenation.

S. Oda, M. Krische, Brannon Sam, 2015, Angewandte Chemie.

Highly enantioselective direct reductive coupling of conjugated alkynes and alpha-ketoesters via rhodium-catalyzed asymmetric hydrogenation.

M. Krische, Ming‐Yu Ngai, J. Kong, 2006, Journal of the American Chemical Society.

Phosphine-catalyzed regiospecific allylic amination and dynamic kinetic resolution of Morita-Baylis-Hillman acetates.

M. Krische, J. Kong, C. Cho, 2004, Organic letters.

Regio- and stereoselective construction of gamma-butenolides through phosphine-catalyzed substitution of Morita-Baylis-Hillman acetates: an organocatalytic allylic alkylation.

M. Krische, C. Cho, 2004, Angewandte Chemie.

Highly enantioselective reductive cyclization of acetylenic aldehydes via rhodium catalyzed asymmetric hydrogenation.

M. Krische, J. Rhee, 2006, Journal of the American Chemical Society.

Regio- and diastereoselective C-C coupling of α-olefins and styrenes to 3-hydroxy-2-oxindoles by Ru-catalyzed hydrohydroxyalkylation.

M. Krische, J. Mowat, E. Yamaguchi, 2013, Angewandte Chemie.

Sustainable catalysis : challenges and practices for the pharmaceutical and fine chemical industries

K. K. Hii, M. T. Williams, M. Krische, 2013 .

Concise stereocontrolled formal synthesis of (+/-)-quinine and total synthesis of (+/-)-7- hydroxyquinine via merged Morita-Baylis-Hillman-Tsuji-Trost cyclization.

Peter A. Webber, M. Krische, P. Webber, 2008, The Journal of organic chemistry.

Enantioselective reductive coupling of 1,3-enynes to heterocyclic aromatic aldehydes and ketones via rhodium-catalyzed asymmetric hydrogenation: mechanistic insight into the role of Brønsted acid additives.

M. Krische, V. Komanduri, 2006, Journal of the American Chemical Society.

Catalytic enone cycloallylation via concomitant activation of latent nucleophilic and electrophilic partners: merging organic and transition metal catalysis.

M. Krische, J. Kong, B. Jellerichs, 2003, Journal of the American Chemical Society.

Asymmetric induction in hydrogen-mediated reductive aldol additions to alpha-amino aldehydes catalyzed by rhodium: selective formation of syn-stereotriads directed by intramolecular hydrogen-bonding.

M. Krische, C. Jung, 2006, Journal of the American Chemical Society.

Phosphine catalyzed alpha-arylation of enones and enals using hypervalent bismuth reagents: regiospecific enolate arylation via nucleophilic catalysis.

Phillip K. Koech, M. Krische, 2004, Journal of the American Chemical Society.

Borane-mediated aldol cycloreduction of monoenone monoketones: diastereoselective formation of quaternary centers.

M. Krische, David F. Cauble, Ryan R. Huddleston, 2003, The Journal of organic chemistry.

Hydrogen-mediated reductive coupling of conjugated alkynes with ethyl (N-Sulfinyl)iminoacetates: synthesis of unnatural alpha-amino acids via rhodium-catalyzed C-C bond forming hydrogenation.

M. Krische, J. Kong, C. Cho, 2005, Journal of the American Chemical Society.

Hydrogen-mediated aldol reductive coupling of vinyl ketones catalyzed by rhodium: high syn-selectivity through the effect of tri-2-furylphosphine.

M. Krische, C. Jung, S. Garner, 2006, Organic letters.

Catalytic addition of metallo-aldehyde enolates to ketones: a new C-C bond-forming hydrogenation.

Phillip K. Koech, M. Krische, 2004, Organic letters.

Ruthenium-catalyzed hydrohydroxyalkylation of acrylates with diols and α-hydroxycarbonyl compounds to form spiro- and α-methylene-γ-butyrolactones.

M. Krische, J. Mowat, A. Waldeck, 2013, Journal of the American Chemical Society.

Catalytic crossed Michael cycloisomerization of thioenoates: total synthesis of (+/-)-ricciocarpin A.

M. Krische, K. Agapiou, 2003, Organic letters.

Asymmetric Ruthenium-Catalyzed Carbonyl Allylations by Gaseous Allene via Hydrogen Auto-Transfer: 1° vs 2° Alcohol Dehydrogenation for Streamlined Polyketide Construction.

M. Krische, Eliezer Ortiz, Brian J. Spinello, 2023, ACS catalysis.

Chiral Amines via Enantioselective π-Allyliridium-C,O-Benzoate-Catalyzed Allylic Alkylation: Student Training via Industrial-Academic Collaboration.

Peng Liu, M. Krische, J. Zbieg, 2022, Accounts of chemical research.

Kinetic, ESI-CID-MS and Computational Studies of π-Allyliridium C,O-Benzoate-Catalyzed Allylic Amination: Understanding the Effect of Cesium Ion.

Binh Khanh Mai, P. Liu, M. Krische, 2022, ACS catalysis.

Protecting-group-free synthesis of 3-tert-prenylated oxindoles: contiguous all-carbon quaternary centers via tertiary neopentyl substitution.

M. Krische, Christopher D. Grant, 2009, Organic letters.

Duplex molecular strands based on the 3,6-diaminopyridazine hydrogen bonding motif: amplifying small-molecule self-assembly preferences through preorganization and iterative arrangement of binding residues.

M. Krische, H. Gong, 2005, Journal of the American Chemical Society.

Phosphine-Mediated Reductive Condensation of γ-Acyloxy Butynoates: A Diversity Oriented Strategy for the Construction of Substituted Furans.

M. Krische, Jian-Cheng Wang, C. Jung, 2004 .

Regioselective ruthenium catalyzed hydrohydroxyalkylation of dienes with 3-hydroxy-2-oxindoles: prenylation, geranylation, and beyond.

M. Krische, Te-Yu Chen, 2013, Organic letters.

Thermal Hetero-Diels-Alder Reaction of Benzocyclobutenones with Isatins To Form 2-Oxindole Spirolactones.

Ben W. H. Turnbull, M. Krische, T. Wurm, 2017, The Journal of organic chemistry.

Direct vinylation of alcohols or aldehydes employing alkynes as vinyl donors: a ruthenium catalyzed C-C bond-forming transfer hydrogenation.

M. Krische, Vanessa M. Williams, M. Chaulagain, 2009, Journal of the American Chemical Society.

Interconversion of single and double helices formed from synthetic molecular strands

Ivan Huc, Michael J. Krische, Jean-Marie Lehn, 2000, Nature.

Ruthenium-catalyzed insertion of adjacent diol carbon atoms into C-C bonds: Entry to type II polyketides

Ben W. H. Turnbull, M. Krische, Brett R. Ambler, 2017, Science.

The Palladium-Catalyzed Enyne Cycloisomerization Reaction in a General Approach to the Asymmetric Syntheses of the Picrotoxane Sesquiterpenes. Part I. First-Generation Total Synthesis of Corianin and Formal Syntheses of Picrotoxinin and Picrotin

B. Trost, Andrew P Thomas, M. Krische, 1999 .

Modular Terpenoid Construction via Catalytic Enantioselective Formation of All-Carbon Quaternary Centers: Total Synthesis of Oridamycin A, Triptoquinones B and C, and Isoiresin.

Jiajie Feng, M. Krische, F. Noack, 2016, Journal of the American Chemical Society.

Enantioselective iridium-catalyzed imine vinylation: optically enriched allylic amines via alkyne-imine reductive coupling mediated by hydrogen.

M. Krische, Ming‐Yu Ngai, A. Barchuk, 2007, Journal of the American Chemical Society.

Enantioselective reductive coupling of acetylene to N-arylsulfonyl imines via rhodium catalyzed C-C bond-forming hydrogenation: (Z)-dienyl allylic amines.

M. Krische, J. Kong, E. Skucas, 2007, Journal of the American Chemical Society.

Diastereo- and enantioselective catalytic carbometallative aldol cycloreduction: tandem conjugate addition-aldol cyclization.

M. Krische, David F. Cauble, John D. Gipson, 2003, Journal of the American Chemical Society.

Conversion of Primary Alcohols and Butadiene to Branched Ketones via Merged Transfer Hydrogenative Carbonyl Addition-Redox Isomerization Catalyzed by Rhodium.

M. Krische, Jessica Y. Wu, Brian J. Spinello, 2021, Journal of the American Chemical Society.

Enantioselective Iridium-Catalyzed Allylation of Acetylenic Ketones via 2-Propanol-Mediated Reductive Coupling of Allyl Acetate: C14-C23 of Pladienolide D.

M. Krische, Minji Yoo, G. Brito, 2019, Angewandte Chemie.

Catalytic Enantioselective Allylations of Acetylenic Aldehydes via 2-Propanol-Mediated Reductive Coupling.

S. Rychnovsky, M. Krische, R. Pilli, 2018, Organic letters.

Nickel-Catalyzed Cross-Coupling of Vinyl Dioxanones to Form Enantiomerically Enriched Cyclopropanes.

S. W. Kim, M. Krische, Yian Guo, 2017, Journal of the American Chemical Society.

Catalytic Enantioselective Grignard Nozaki—Hiyama Methallylation from the Alcohol Oxidation Level: Chloride Compensates for π-Complex Instability.

M. Krische, Abbas Hassan, I. Townsend, 2012 .

Enantioselective Ruthenium-BINAP-Catalyzed Carbonyl Reductive Coupling of Alkoxyallenes: Convergent Construction of syn-sec,tert-Diols via (Z)-σ-Allylmetal Intermediates.

M. Krische, M. Xiang, Dana E Pfaffinger, 2021, Journal of the American Chemical Society.

Direct Conversion of Primary Alcohols to 1,2-Amino Alcohols: Enantioselective Iridium-Catalyzed Carbonyl Reductive Coupling of Phthalimido-Allene via Hydrogen Auto-Transfer.

M. Krische, M. Xiang, Leyah A. Schwartz, 2019, Journal of the American Chemical Society.

Total Synthesis of Clavosolide A via Asymmetric Alcohol-Mediated Carbonyl Allylation: Beyond Protecting Groups or Chiral Auxiliaries in Polyketide Construction.

M. Krische, James M Cabrera, 2019, Angewandte Chemie.

Successive Nucleophilic and Electrophilic Allylation for the Catalytic Enantioselective Synthesis of 2,4-Disubstituted Pyrrolidines.

M. Krische, Guoshun Luo, M. Xiang, 2019, Organic letters.

Ruthenium-BINAP Catalyzed Alcohol C-H tert-Prenylation via 1,3-Enyne Transfer Hydrogenation: Beyond Stoichiometric Carbanions in Enantioselective Carbonyl Propargylation.

M. Krische, D. Herkommer, K. D. Nguyen, 2016, Journal of the American Chemical Society.

Diastereo- and Enantioselective Iridium Catalyzed Carbonyl (α-Cyclopropyl)allylation via Transfer Hydrogenation.

M. Krische, Suckchang Hong, R. Tsutsumi, 2015, Chemistry.

Enantioselective ruthenium-catalyzed carbonyl allylation via alkyne-alcohol C-C bond-forming transfer hydrogenation: allene hydrometalation vs oxidative coupling.

M. Krische, K. D. Nguyen, Wandi Zhang, 2015, Journal of the American Chemical Society.

Alkynes as Allylmetal Equivalents in Redox-Triggered C–C Couplings to Primary Alcohols: (Z)-Homoallylic Alcohols via Ruthenium-Catalyzed Propargyl C–H Oxidative Addition

M. Krische, K. D. Nguyen, Boyoung Y. Park, 2014, Journal of the American Chemical Society.

Enantioselective carbonyl propargylation by iridium-catalyzed transfer hydrogenative coupling of alcohols and propargyl chlorides.

M. Krische, Laina M. Geary, S. Woo, 2012, Angewandte Chemie.

Diastereo- and enantioselective iridium-catalyzed carbonyl propargylation from the alcohol or aldehyde oxidation level: 1,3-enynes as allenylmetal equivalents.

Joyce C. Leung, M. Krische, Laina M. Geary, 2012, Angewandte Chemie.

Polarity inversion of donor-acceptor cyclopropanes: disubstituted δ-lactones via enantioselective iridium catalysis.

M. Krische, J. Moran, Austin G. Smith, 2011, Journal of the American Chemical Society.

Diene hydroacylation from the alcohol or aldehyde oxidation level via ruthenium-catalyzed C-C bond-forming transfer hydrogenation: synthesis of beta,gamma-unsaturated ketones.

M. Krische, J. Bower, F. Shibahara, 2008, Journal of the American Chemical Society.

Carbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: a ruthenium-catalyzed C-C bond-forming transfer hydrogenation.

M. Krische, J. Bower, Vanessa M. Williams, 2008, Angewandte Chemie.

Catalytic C-C coupling via transfer hydrogenation: reverse prenylation, crotylation, and allylation from the alcohol or aldehyde oxidation level.

M. Krische, J. Bower, J. F. Bower, 2007, Journal of the American Chemical Society.

Historical perspective on ruthenium-catalyzed hydrogen transfer and survey of enantioselective hydrogen auto-transfer processes for the conversion of lower alcohols to higher alcohols

M. Krische, Jon Shezaf, Eliezer Ortiz, 2022, Chemical science.

Regio- and Enantioselective Iridium-Catalyzed Amination of Alkyl-Substituted Allylic Acetates with Secondary Amines.

M. Krische, J. Zbieg, C. Stivala, 2021, Organic letters.

Understanding Halide Counterion Effects in Enantioselective Ruthenium-Catalyzed Carbonyl (α-Aryl)allylation: Alkynes as Latent Allenes and Trifluoroethanol-Enhanced Turnover in The Conversion of Ethanol to Higher Alcohols via Hydrogen Auto-transfer.

Théo P. Gonçalves, Yu-Hsiang Chang, Kuo‐Wei Huang, 2021, Journal of the American Chemical Society.

Total Synthesis of the Spliceosome Modulator Pladienolide B via Asymmetric Alcohol-Mediated syn- and anti-Diastereoselective Carbonyl Crotylation.

M. Krische, Minji Yoo, 2021, Angewandte Chemie.

Formate-Mediated Cross-Electrophile Reductive Coupling of Aryl Iodides and Bromopyridines.

M. Krische, R. A. Swyka, M. Xiang, 2020, Israel journal of chemistry.

Inversion of Enantioselectivity in Allene Gas versus Allyl Acetate Reductive Aldehyde Allylation Guided by Metal-Centered Stereogenicity: An Experimental and Computational Study.

Binh Khanh Mai, S. W. Kim, Peng Liu, 2019, ACS catalysis.

Vinyl Triflate-Aldehyde Reductive Coupling-Redox Isomerization Mediated by Formate: Rhodium-Catalyzed Ketone Synthesis in the Absence of Stoichiometric Metals.

M. Krische, R. A. Swyka, William G Shuler, 2019, Chemistry.

Total Synthesis and Structural Validation of Phosdiecin A via Asymmetric Alcohol-Mediated Carbonyl Reductive Coupling.

Ariel M. Sarotti, M. Krische, R. Pilli, 2019, Journal of the American Chemical Society.

Regio- and Enantioselective Iridium-Catalyzed N-Allylation of Indoles and Related Azoles with Racemic Branched Alkyl-Substituted Allylic Acetates.

S. W. Kim, M. Krische, J. Zbieg, 2019, Angewandte Chemie.

Conversion of Aldehydes to Branched or Linear Ketones via Regiodivergent Rhodium-Catalyzed Vinyl Bromide Reductive Coupling-Redox Isomerization Mediated by Formate.

M. Krische, R. A. Swyka, Wandi Zhang, 2019, Journal of the American Chemical Society.

Catalytic Enantioselective Synthesis of Chiral Organofluorine Compounds: Alcohol-Mediated Hydrogen Transfer for Catalytic Carbonyl Reductive Coupling.

M. Krische, J. Tauber, Leyah A. Schwartz, 2019, Organic process research & development.

Cyclometalated Iridium-PhanePhos Complexes Are Active Catalysts in Enantioselective Allene-Fluoral Reductive Coupling and Related Alcohol-Mediated Carbonyl Additions That Form Acyclic Quaternary Carbon Stereocenters.

Théo P. Gonçalves, Kuo‐Wei Huang, M. Krische, 2019, Journal of the American Chemical Society.

Enantioselective iridium-catalyzed carbonyl isoprenylation via alcohol-mediated hydrogen transfer.

M. Krische, Guoshun Luo, M. Xiang, 2019, Chemical communications.

Regio- and Enantioselective Iridium-Catalyzed Amination of Racemic Branched Alkyl-Substituted Allylic Acetates with Primary and Secondary Aromatic and Heteroaromatic Amines.

S. W. Kim, M. Krische, J. Zbieg, 2018, Journal of the American Chemical Society.

Catalytic Enantioselective Carbonyl Propargylation Beyond Preformed Carbanions: Reductive Coupling and Hydrogen Auto‐Transfer

M. Krische, S. Woo, Brett R. Ambler, 2018, ChemCatChem.

Alternating oligo(o,p-phenylenes) via ruthenium catalyzed diol–diene benzannulation: orthogonality to cross-coupling enables de novo nanographene and PAH construction† †Electronic supplementary information (ESI) available: Experimental procedures and spectroscopic data for all new compounds (1H NMR,

S. Roberts, M. Krische, J. Nie, 2018, Chemical science.

Asymmetric Allylation of Glycidols Mediated by Allyl Acetate via Iridium-Catalyzed Hydrogen Transfer.

S. W. Kim, M. Krische, Wonchul Lee, 2017, Organic letters.

Metal-catalyzed reductive coupling of olefin-derived nucleophiles: Reinventing carbonyl addition

M. Krische, K. D. Nguyen, Boyoung Y. Park, 2016, Science.

Iridium-Catalyzed C—C Coupling of a Simple Propargyl Ether with Primary Alcohols: Enantioselective Homoaldol Addition via Redox-Triggered (Z)-Siloxyallylation.

M. Krische, Wandi Zhang, T. Liang, 2016 .

Ruthenium-Catalyzed Transfer Hydrogenation for C–C Bond Formation: Hydrohydroxyalkylation and Hydroaminoalkylation via Reactant Redox Pairs

S. Oda, M. Krische, Laina M. Geary, 2016, Topics in Current Chemistry.

Ruthenium Catalyzed Diastereo- and Enantioselective Coupling of Propargyl Ethers with Alcohols: Siloxy-Crotylation via Hydride Shift Enabled Conversion of Alkynes to π-Allyls.

M. Krische, K. D. Nguyen, Te-Yu Chen, 2015, Journal of the American Chemical Society.

Enantioselective Ruthenium‐Catalyzed Carbonyl Allylation via Alkyne—Alcohol C—C Bond‐Forming Transfer Hydrogenation: Allene Hydrometalation vs. Oxidative Coupling.

M. Krische, K. D. Nguyen, Wandi Zhang, 2015 .

Paraformaldehyde and Methanol as C1 Feedstocks in Metal‐Catalyzed C—C Couplings of π‐Unsaturated Reactants: Beyond Hydroformylation

M. Krische, B. Breit, Brannon Sam, 2015 .

Catalytic Enantioselective C—H Functionalization of Alcohols by Redox‐Triggered Carbonyl Addition: Borrowing Hydrogen, Returning Carbon

M. Krische, John M. Ketcham, T. Montgomery, 2014 .

Asymmetric alcohol C-H allylation and syn-crotylation: C9-C20 of tetrafibricin.

M. Krische, T. Itoh, T. Montgomery, 2014, Organic letters.

Chiral‐Anion‐Dependent Inversion of Diastereo‐ and Enantioselectivity in Carbonyl Crotylation via Ruthenium‐Catalyzed Butadiene Hydrohydroxyalkylation.

M. Krische, E. Yamaguchi, E. McInturff, 2013 .

Iridium‐Catalyzed Allylation of Chiral β‐Stereogenic Alcohols: Bypassing Discrete Formation of Epimerizable Aldehydes.

M. Krische, Daniel C. Schmitt, Anne-Marie R. Dechert-Schmitt, 2013 .

Enantioselective Carbonyl Allylation and Crotylation from the Alcohol Oxidation Level via C–C Bond Forming Transfer Hydrogenation

M. Krische, J. Moran, 2013 .

Site-Selective Primary Alcohol Dehydrogenation Enables Protecting Group-Free Diastereoselective C-C Coupling of 1,3- Glycols and Allyl Acetate**

M. Krische, Daniel C. Schmitt, Dr. Anne-Marie R. Dechert-Schmitt, 2013 .

Ruthenium-catalyzed reductive coupling of 1,3-enynes and aldehydes by transfer hydrogenation: anti-diastereoselective carbonyl propargylation.

Joyce C. Leung, M. Krische, Laina M. Geary, 2012, Chemistry.

Formation of C–C bonds via ruthenium-catalyzed transfer hydrogenation

M. Krische, J. Moran, 2012, Pure and applied chemistry. Chimie pure et appliquee.

Enantioselective Iridium‐Catalyzed Carbonyl Allylation from the Alcohol Oxidation Level via Transfer Hydrogenation: Minimizing Pre‐Activation for Synthetic Efficiency

M. Krische, S. Han, I. Kim, 2010 .

anti-Diastereo- and Enantioselective Carbonyl Crotylation from the Alcohol or Aldehyde Oxidation Level Employing a Cyclometalated Iridium Catalyst: α-Methyl Allyl Acetate as a Surrogate to Preformed Crotylmetal Reagents.

M. Krische, S. Han, I. Kim, 2009 .

Direct Vinylation of Alcohols or Aldehydes Employing Alkynes as Vinyl Donors: A Ruthenium-Catalyzed C—C Bond-Forming Transfer Hydrogenation.

M. Krische, Vanessa M. Williams, M. Chaulagain, 2009 .

Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.

M. Krische, J. Bower, F. Shibahara, 2008, Journal of the American Chemical Society.

Reductive C-C Coupling via Hydrogenation and Transfer Hydrogenation: Departure from Stoichiometric Metals in Carbonyl Addition.

M. Krische, J. Roane, Michael R. Holmes, 2017, Current opinion in green and sustainable chemistry.

Diastereo- and enantioselective hydrogenative aldol coupling of vinyl ketones: design of effective monodentate TADDOL-like phosphonite ligands.

M. Krische, Hiroki Iida, S. Han, 2008, Journal of the American Chemical Society.

Enantioselective Conversion of Primary Alcohols to α-exo-Methylene γ-Butyrolactones via Iridium-Catalyzed C—C Bond-Forming Transfer Hydrogenation: 2-(Alkoxycarbonyl)allylation.

M. Krische, Abbas Hassan, Boyoung Y. Park, 2013 .

Alkyne-aldehyde reductive C-C coupling through ruthenium-catalyzed transfer hydrogenation: direct regio- and stereoselective carbonyl vinylation to form trisubstituted allylic alcohols in the absence of premetallated reagents.

Joyce C. Leung, M. Krische, Brannon Sam, 2011, Chemistry.

Erratum: Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1,1-Dimethylallene as the prenyl donor (Journal of the American Chemical Society (2009) 131 (6916-6917))

M. Krische, Hoon Han, S. Han, 2010 .

Carbonyl anti-(α-Amino)allylation via Ruthenium Catalyzed Hydrogen Autotransfer: Use of an Acetylenic Pyrrole as an Allylmetal Pronucleophile.

M. Krische, Weijie Chen, Wandi Zhang, 2017, Organic letters.

Ruthenium(0) Catalyzed Endiyne-α-Ketol [4 + 2] Cycloaddition: Convergent Assembly of Type II Polyketide Substructures via C-C Bond Forming Transfer Hydrogenation.

M. Krische, A. Saxena, F. Perez, 2015, Journal of the American Chemical Society.

M. Krische, F. Shibahara, J. F. Bower, 2008, Journal of the American Chemical Society.

Carbonyl allylation in the absence of preformed allyl metal reagents: reverse prenylation via iridium-catalyzed hydrogenative coupling of dimethylallene.

M. Krische, J. Bower, J. F. Bower, 2007, Journal of the American Chemical Society.

A Metallacycle Fragmentation Strategy for Vinyl Transfer from Enol Carboxylates to Secondary Alcohol C-H Bonds via Osmium- or Ruthenium-Catalyzed Transfer Hydrogenation.

M. Krische, Boyoung Y. Park, Tom Luong, 2015, Journal of the American Chemical Society.

ESI-MS, DFT, and synthetic studies on the H(2)-mediated coupling of acetylene: insertion of C=X bonds into rhodacyclopentadienes and Brønsted acid cocatalyzed hydrogenolysis of organorhodium intermediates.

J. Brodbelt, M. Baik, M. Krische, 2009, Journal of the American Chemical Society.

anti-Aminoallylation of aldehydes via ruthenium-catalyzed transfer hydrogenative coupling of sulfonamido allenes: 1,2-aminoalcohols.

M. Krische, J. Zbieg, E. Skucas, 2009, Journal of the American Chemical Society.

Redox-triggered C-C coupling of diols and alkynes: synthesis of β,γ-unsaturated α-hydroxyketones and furans by ruthenium-catalyzed hydrohydroxyalkylation.

M. Krische, K. D. Nguyen, E. McInturff, 2014, Angewandte Chemie.

Enantioselective Reductive Coupling of 1,3-Enynes to Glyoxalates Mediated by Hydrogen: Asymmetric Synthesis of β,γ-Unsaturated α-Hydroxy Esters

Young‐Taek Hong, M. Krische, C. Cho, 2007 .

Rhodium-catalyzed reductive mannich coupling of vinyl ketones to N-sulfonylimines mediated by hydrogen.

M. Krische, S. Garner, 2007, The Journal of organic chemistry.

Allylic amines via iridium-catalyzed C-C bond forming hydrogenation: imine vinylation in the absence of stoichiometric byproducts or metallic reagents.

M. Krische, Ming‐Yu Ngai, A. Barchuk, 2007, Journal of the American Chemical Society.

Iridium-catalyzed C-C bond forming hydrogenation: direct regioselective reductive coupling of alkyl-substituted alkynes to activated ketones.

M. Krische, Ming‐Yu Ngai, A. Barchuk, 2007, Journal of the American Chemical Society.

Alpha-hydroxy esters via enantioselective hydrogen-mediated C-C coupling: regiocontrolled reactions of silyl-substituted 1,3-diynes.

M. Krische, C. Cho, 2006, Organic letters.

A New catalytic C[bond]C bond-forming hydrogenation: reductive coupling of dienes and glyoxals under catalytic hydrogenation conditions.

Hye‐Young Jang, M. Krische, Ryan R. Huddleston, 2003, Angewandte Chemie.

Ring expansion of cyclic 1,2-diols to form medium sized rings via ruthenium catalyzed transfer hydrogenative [4+2] cycloaddition.

M. Krische, Laina M. Geary, Zachary A. Kasun, 2014, Chemical communications.

Ruthenium catalyzed hydroaminoalkylation of isoprene via transfer hydrogenation: byproduct-free prenylation of hydantoins.

M. Krische, Daniel C. Schmitt, E. Yamaguchi, 2013, Chemical communications.

C(21)-C(40) of tetrafibricin via metal catalysis: beyond stoichiometric chiral reagents, auxiliaries, and premetalated nucleophiles.

M. Krische, Esa T. T. Kumpulainen, Byungsoo Kang, 2011, Organic letters.

Hydrogen-mediated C-C bond formation: catalytic regio- and stereoselective reductive condensation of alpha-keto aldehydes and 1,3-enynes.

Hye‐Young Jang, M. Krische, Ryan R. Huddleston, 2004, Journal of the American Chemical Society.

Direct Generation of Triketide Stereopolyads via Merged Redox-Construction Events: Total Synthesis of (+)-Zincophorin Methyl Ester.

M. Krische, Xin Gao, Radosław Lipiński, 2015, Journal of the American Chemical Society.

Total synthesis of 6-deoxyerythronolide B via C-C bond-forming transfer hydrogenation.

M. Krische, Xin Gao, S. Woo, 2013, Journal of the American Chemical Society.

Synthesis of the cytotrienin A core via metal catalyzed C-C coupling.

M. Krische, David J Del Valle, Michael Rössle, 2011, Organic letters.

Ruthenium-catalyzed C-C coupling of amino alcohols with dienes via transfer hydrogenation: redox-triggered imine addition and related hydroaminoalkylations.

M. Krische, T. Montgomery, I. Volchkov, 2015, Journal of the American Chemical Society.

Direct, redox-neutral prenylation and geranylation of secondary carbinol C-H bonds: C4-regioselectivity in ruthenium-catalyzed C-C couplings of dienes to α-hydroxy esters.

Joyce C. Leung, M. Krische, J. Zbieg, 2012, Journal of the American Chemical Society.

Direct ruthenium-catalyzed C-C coupling of ethanol: diene hydro-hydroxyethylation to form all-carbon quaternary centers.

M. Krische, Hoon Han, 2010, Organic letters.

Allenamide hydro-hydroxyalkylation: 1,2-amino alcohols via ruthenium-catalyzed carbonyl anti-aminoallylation.

M. Krische, J. Zbieg, E. McInturff, 2010, Organic letters.

Iridium‐Catalyzed anti‐Diastereo‐ and Enantioselective Carbonyl (α‐Trifluoromethyl)allylation from the Alcohol or Aldehyde Oxidation Level.

M. Krische, Xin Gao, Yong Jian Zhang, 2011 .

A diastereoselective metal-catalyzed [2+2] cycloaddition of bis-enomes.

M. Krische, T. Baik, Longcheng Wang, 2001, Journal of the American Chemical Society.

Diols as Dienophiles: Bridged Carbocycles via Ruthenium(0)-Catalyzed Transfer Hydrogenative Cycloadditions of Cyclohexadiene or Norbornadiene.

K. Fukaya, M. Krische, Hiroki Sato, 2017, Angewandte Chemie.

On asymmetric induction in allylic alkylation via enantiotopic facial discrimination

B. Trost, M. Krische, G. Zanoni, 1996 .

Phosphine-catalyzed allylic substitution of Morita-Baylis-Hillman acetates: synthesis of N-protected beta-aminophosphonic acid esters.

M. Krische, Haeil Park, C. Cho, 2006, The Journal of organic chemistry.

Enantioselective Iridium‐Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level via Transfer Hydrogenation Coupling of Allyl Acetate: Departure from Chirally Modified Allyl Metal Reagents in Carbonyl Addition.

M. Krische, I. Kim, Ming‐Yu Ngai, 2009 .

Chiral β-diketonate ligands of ‘pseudo planar chiral’ topology: enantioselective synthesis and transition metal complexation

M. Krische, Longcheng Wang, B. M. Bocknack, 2005 .

Royal Society of Chemistry Awards 2015.

A. P. Alivisatos, H. Overkleeft, Chi‐Huey Wong, 2015, Angewandte Chemie.

Palladium-Catalyzed Enyne Cycloisomerization Reaction in an Asymmetric Approach to the Picrotoxane Sesquiterpenes. 2. Second-Generation Total Syntheses of Corianin, Picrotoxinin, Picrotin, and Methyl Picrotoxate

B. Trost, M. Krische, 1999 .

Hydroamination versus Allylic Amination in Iridium-Catalyzed Reactions of Allylic Acetates with Amines: 1,3-Aminoalcohols via Ester-Directed Regioselectivity.

S. W. Kim, M. Krische, J. Zbieg, 2018, Journal of the American Chemical Society.

Iridium-catalyzed hydrocarboxylation of 1,1-dimethylallene: byproduct-free reverse prenylation of carboxylic acids.

M. Krische, I. Kim, 2008, Organic letters.

Diastereoselective cobalt-catalyzed aldol and Michael cycloreductions.

M. Krische, T. Baik, L. C. Wang, 2001, Journal of the American Chemical Society.

Regioselective Hydrohydroxyalkylation of Styrene with Primary Alcohols or Aldehydes via Ruthenium-Catalyzed C-C Bond Forming Transfer Hydrogenation.

M. Krische, Gang‐Wei Wang, Hongde Xiao, 2016, Angewandte Chemie.

Branch-selective reductive coupling of 2-vinyl pyridines and imines via rhodium catalyzed C-C bond forming hydrogenation.

M. Krische, V. Komanduri, Christopher D. Grant, 2008, Journal of the American Chemical Society.

γ-Amino-β-keto Phosphonates in Synthesis: Synthesis of the Sphingosine Skeleton

M. Krische, A. Koskinen, 1990 .

Reductive aldol coupling of divinyl ketones via rhodium-catalyzed hydrogenation: syn-diastereoselective construction of beta-hydroxyenones.

M. Krische, S. Han, 2006, Organic letters.

Diastereo- and Enantioselective Reductive Aldol Addition of Vinyl Ketones via Catalytic Hydrogenation.

M. Krische, S. Han, Abbas Hassan, 2008, Synthesis.

Metal‐Catalyzed Reductive Aldol Coupling

M. Krische, S. Han, S. Garner, 2008 .

The first direct and enantioselective cross-aldol reaction of aldehydes

M. Krische, David F. Cauble, 2002 .

Reductive generation of enolates from enones using elemental hydrogen: catalytic C-C bond formation under hydrogenative conditions.

Hye‐Young Jang, M. Krische, Ryan R. Huddleston, 2002, Journal of the American Chemical Society.

Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level Using Allyl Acetate as an Allyl Metal Surrogate.

M. Krische, I. Kim, Ming‐Yu Ngai, 2008 .

9‐Bromo‐9‐Phenylfluorene

T. Jamison, W. Lubell, M. Krische, 2003 .

Enantioselective Iridium-Catalyzed Reductive Coupling of Dienes with Oxetanones and N-Acyl-Azetidinones Mediated by 2-Propanol.

M. Krische, Cole C. Meyer, Zachary J Dubey, 2022, Angewandte Chemie.

Hydrogenation and Transfer Hydrogenation

M. Krische, Yong-kui Sun, 2007 .

Polyketide construction via hydrohydroxyalkylation and related alcohol C-H functionalizations: reinventing the chemistry of carbonyl addition.

M. Krische, T. Itoh, Daniel C. Schmitt, 2014, Natural product reports.

The Utilization of Persistent H-Bonding Motifs in the Self-Assembly of Supramolecular Architectures

J. Lehn, M. Krische, 2000 .

The covalent casting of one-dimensional hydrogen bonding motifs: toward oligomers and polymers of predefined topography.

M. Krische, E. A. Archer, A. E. Sochia, 2001, Chemistry.

Hydrogen Bonding in Noncovalent Synthesis: Selectivity and the Directed Organization of Molecular Strands

M. Krische, E. A. Archer, H. Gong, 2001 .

Supramolecular polymers generated from heterocomplementary monomers linked through multiple hydrogen-bonding arrays--formation, characterization, and properties.

J. Lehn, M. Schmutz, V. Berl, 2002, Chemistry.

Self-assembly of helical supramolecular channels from chiral aminopyrimidine hydrogen bonding motifs in the solid state

J. Lehn, M. Krische, E. Cheung, 1999 .

Helical Rod-like Phenylene Cages via Ruthenium Catalyzed Diol-Diene Benzannulation: A Cord of Three Strands.

S. Roberts, M. Krische, J. A. Bender, 2018, Journal of the American Chemical Society.

Enantiomeric separations of chiral sulfonic and phosphoric acids with barium-doped cyclofructan selectors via an ion interaction mechanism.

D. Armstrong, M. Krische, Zhaobin Han, 2014, Analytical chemistry.

Successive C-C coupling of dienes to vicinally dioxygenated hydrocarbons: ruthenium catalyzed [4 + 2] cycloaddition across the diol, hydroxycarbonyl, or dione oxidation levels.

Ben W. Glasspoole, M. Krische, Laina M. Geary, 2013, Journal of the American Chemical Society.

Cross-metathesis–based approaches to heteroaromatics: Combining catalysts for furan formation

M. Krische, 2010, Proceedings of the National Academy of Sciences.

MOLECULAR-RECOGNITION-DIRECTED SELF-ASSEMBLY OF PLEATED SHEETS FROM 2-AMINOPYRIMIDINE HYDROGEN-BONDING MOTIFS

J. Lehn, J. Fischer, M. Krische, 1998 .

Enantioselective Iridium-Catalyzed Allylation of Nitroalkanes: Entry to β-Stereogenic α-Quaternary Primary Amines.

Binh Khanh Mai, S. W. Kim, Peng Liu, 2021, Journal of the American Chemical Society.

Peptide-Based Materials

C. Hunter, K. Houk, R. Naaman, 2012 .

Hydrogen-bond-mediated self-assembly of aminopyrazolones: macrocyclic quartets-single and stacked one-dimensional motifs.

M. Krische, H. Gong, 2005, Angewandte Chemie.

Hypervalent Iodine Chemistry: Modern Developments in Organic Synthesis. Topics in Current Chemistry, 224 Edited by T. Wirth (Cardiff University). Springer-Verlag: Berlin, Heidelberg, New York. 2003. x + 264 pp. $189.00. ISBN 3-540-44107-7.

M. Krische, 2003 .

Ruthenium catalyzed hydrohydroxyalkylation of isoprene with heteroaromatic secondary alcohols: isolation and reversible formation of the putative metallacycle intermediate.

M. Krische, Boyoung Y. Park, T. Montgomery, 2013, Journal of the American Chemical Society.

Unimolecular and Supramolecular Electronics II: Chemistry and Physics Meet at Metal-Molecule Interfaces

C. Hunter, M. Ratner, K. Houk, 2012 .

Total synthesis of methyl picrotoxate via the palladium catalyzed enyne cycloisomerization reaction

B. Trost, M. Krische, 1998 .

Duplex oligomers defined via covalent casting of a one-dimensional hydrogen-bonding motif.

M. Krische, E. A. Archer, 2002, Journal of the American Chemical Society.

Hierarchic supramolecular interactions within assemblies in solution and in the crystal of 2,3,6,7-tetrasubstituted 5,5′-(anthracene-9,10-diyl) bis[pyrimidin-2-amines]

T. Balaban, J. Lehn, A. Eichhöfer, 2006 .

Nanostructured Polymer Duplexes via the Covalent Casting of 1-Dimensional H-Bonding Motifs: A New Strategy for the Self-Assembly of Macromolecular Precursors

M. Krische, E. A. Archer, A. V. Lynch, 2000 .

Second generation light-driven molecular motors: Unidirectional rotation controlled by a single stereogenic center with near-perfect photoequilibria and acceleration of the speed of rotation by structural modification

M. Krische, E. A. Archer, 2002 .

Self-assembly of 1- and 2-Dimensional Multicompartmental Arrays via the 2-Aminopyrimidine H-Bonding Motif and Selective Guest Inclusion

K. Rissanen, J. Lehn, E. Wegelius, 2000 .

Alkaloid Synthesis

M. Venturi, R. Naaman, D. Beratan, 2012 .

Direct Prenylation of Aromatic and α,β-Unsaturated Carboxamides via Iridium-Catalyzed C—H Oxidative Addition—Allene Insertion.

M. Krische, Yong Jian Zhang, E. Skucas, 2010 .

Anion radical [2 + 2] cycloaddition as a mechanistic probe: stoichiometry- and concentration-dependent partitioning of electron-transfer and alkylation pathways in the reaction of the Gilman reagent Me2CuLi.LiI with bis(enones).

M. Krische, A. J. Berro, N. L. Bauld, 2004, The Journal of organic chemistry.

O-Acetyl 1,3-Propanediol as an Acrolein Proelectrophile in Enantioselective Iridium-Catalyzed Carbonyl Allylation.

M. Krische, Cole C. Meyer, Woo‐Ok Jung, 2023, Organic letters.

Allyl Alcohol as an Acrolein Equivalent in Enantioselective C-C Coupling: Total Synthesis of Amphidinolides R, J, and S.

M. Krische, Cole C. Meyer, Woo‐Ok Jung, 2023, Journal of the American Chemical Society.

Studies on the enantioselective catalysis of photochemically promoted transformations: "sensitizing receptors" as chiral catalysts.

V. Lynch, M. Krische, David F. Cauble, 2003, The Journal of organic chemistry.

Dual Ruthenium-Catalyzed Alkene Isomerization-Hydrogen Auto-Transfer Unlocks Skipped Dienes as Pronucleophiles for Enantioselective Alcohol C-H Allylation.

M. Krische, Weijia Shen, Zachary J Dubey, 2023, Journal of the American Chemical Society.

Transformations of the picrotoxanes: The synthesis of corianin and structural analogues from picrotoxinin

B. Trost, M. Krische, 1998 .

Second generation light-driven molecular motors

Michael J. Krische, M. Krische, E. A. Archer, 2002 .

Metallo-aldehyde enolates via enal hydrogenation: catalytic cross aldolization with glyoxal partners as applied to the synthesis of 3,5-disubstituted pyridazines.

Hye‐Young Jang, M. Krische, G. Marriner, 2004, Journal of Organic Chemistry.

Enones as Latent Enolates in Catalytic Processes: Catalytic Cycloreduction, Cycloaddition and Cycloisomerization

M. Krische, Ryan R. Huddleston, 2003 .

Metallo‐Aldehyde Enolates via Enal Hydrogenation: Catalytic Cross Aldolization with Glyoxal Partners as Applied to the Synthesis of 3,5‐Disubstituted Pyridazines.

Hye‐Young Jang, M. Krische, G. Marriner, 2004 .

Intermolecular Metal-Catalyzed C–C Coupling of Unactivated Alcohols or Aldehydes for Convergent Ketone Construction beyond Premetalated Reagents

M. Krische, Eliezer Ortiz, Brian J. Spinello, 2023, ACS Catalysis.

Metal catalyzed reductive C-C bond formation : a departure from preformed organometallic reagents

M. Krische, B. Breit, 2007 .

Ruthenium‐BINAP Catalyzed Alcohol C—H tert‐Prenylation via 1,3‐Enyne Transfer Hydrogenation: Beyond Stoichiometric Carbanions in Enantioselective Carbonyl Propargylation.

M. Krische, D. Herkommer, K. Nguyen, 2016 .

EPR Spectroscopy: Applications in Chemistry and Biology

C. Hunter, B. Kirchner, S. Ley, 2012 .

Enantioselective Transfer Hydrogenative Cycloaddition Unlocks the Total Synthesis of SF2446 B3: An Aglycone of Arenimycin and SF2446 Type II Polyketide Antibiotics.

M. Krische, T. Hodík, Nancy O. Huynh, 2023, Journal of the American Chemical Society.

Oxetane-, Azetidine-, and Bicyclopentane-Bearing N-Heterocycles from Ynones: Scaffold Diversification via Ruthenium-Catalyzed Oxidative Alkynylation.

M. Krische, Madeline M Evarts, Zachary H Strong, 2023, Organic letters.

Ruthenium-Catalyzed C-C Coupling of Terminal Alkynes with Primary Alcohols or Aldehydes: α,β-Acetylenic Ketones (Ynones) via Oxidative Alkynylation.

M. Krische, Jon Shezaf, Eliezer Ortiz, 2023, Angewandte Chemie.

Carbonyl Allylation and Crotylation: Historical Perspective, Relevance to Polyketide Synthesis, and Evolution of Enantioselective Ruthenium-Catalyzed Hydrogen Auto-Transfer Processes

M. Krische, Jessica Y. Wu, Eliezer Ortiz, 2022, Synthesis.

Chiral-at-Ruthenium-SEGPHOS Catalysts Display Diastereomer-Dependent Regioselectivity: Enantioselective Isoprene-Mediated Carbonyl tert-Prenylation via Halide Counterion Effects.

M. Krische, K. Sakata, Jon Shezaf, 2023, Journal of the American Chemical Society.

Metal Catalyzed Reductive C–C Bond Formation

M. Krische, 2007 .

Protecting-group-free diastereoselective C-C coupling of 1,3-glycols and allyl acetate through site-selective primary alcohol dehydrogenation.

M. Krische, Daniel C. Schmitt, Anne-Marie R. Dechert-Schmitt, 2013, Angewandte Chemie.

1,n-glycols as dialdehyde equivalents in iridium-catalyzed enantioselective carbonyl allylation and iterative two-directional assembly of 1,3-polyols.

M. Krische, Abbas Hassan, I. Kim, 2009, Angewandte Chemie.

Total Synthesis of (+)-SCH 351448: Efficiency via Chemoselectivity and Redox-Economy Powered by Metal Catalysis.

M. Krische, Gang‐Wei Wang, 2016, Journal of the American Chemical Society.

Enantioselective Alcohol C-H Functionalization for Polyketide Construction: Unlocking Redox-Economy and Site-Selectivity for Ideal Chemical Synthesis.

Jiajie Feng, M. Krische, Zachary A. Kasun, 2016, Journal of the American Chemical Society.

Application of a high-throughput enantiomeric excess optical assay involving a dynamic covalent assembly: parallel asymmetric allylation and ee sensing of homoallylic alcohols

E. Anslyn, M. Krische, Hyunjong Jo, 2015, Chemical science.

Total synthesis of cyanolide A in the absence of protecting groups, chiral auxiliaries, or premetalated carbon nucleophiles.

M. Krische, A. Waldeck, 2013, Angewandte Chemie.

Chiral-anion-dependent inversion of diastereo- and enantioselectivity in carbonyl crotylation via ruthenium-catalyzed butadiene hydrohydroxyalkylation.

M. Krische, E. Yamaguchi, E. McInturff, 2012, Journal of the American Chemical Society.

Acyclic Quaternary Carbon Stereocenters via Enantioselective Transition Metal Catalysis.

Jiajie Feng, M. Krische, Michael R. Holmes, 2017, Chemical reviews.

Diastereo- and Enantioselective Iridium Catalyzed Carbonyl (α-Cyclopropyl)allylation via Transfer Hydrogenation.

M. Krische, Suckchang Hong, Ryosuke Tsutsumi, 2015, Chemistry.

M. Krische, V. Komanduri, 2006, Journal of the American Chemical Society.

Ruthenium-Catalyzed Cycloadditions to Form Five-, Six-, and Seven-Membered Rings.

Rosalie S. Doerksen, M. Krische, T. Hodík, 2021, Chemical reviews.

Redox-Triggered C–C Coupling of Alcohols and Vinyl Epoxides: Diastereo- and Enantioselective Formation of All-Carbon Quaternary Centers via tert-(Hydroxy)-Prenylation

Jiajie Feng, M. Krische, Victoria J. Garza, 2014, Journal of the American Chemical Society.

Enantioselective Formation of All-Carbon Quaternary Centers via C-H Functionalization of Methanol: Iridium-Catalyzed Diene Hydrohydroxymethylation.

M. Krische, K. Nguyen, Daniel Herkommer, 2016, Journal of the American Chemical Society.

Leveraging the Stereochemical Complexity of Octahedral Diastereomeric-at-Metal Catalysts to Unlock Regio-, Diastereo-, and Enantioselectivity in Alcohol-Mediated C-C Couplings via Hydrogen Transfer.

Peng Liu, M. Krische, Kuo‐Wei Huang, 2024, Journal of the American Chemical Society.

M. Krische, James M. Cabrera, J. Tauber, 2018, Journal of the American Chemical Society.