Synthetic approaches to 1,4-dicarbonyl compounds

[1]  Weiping Zhou,et al.  Synthesis of Cyclopentenones with C4-Quaternary Stereocenters via Stereospecific [3,3]-Sigmatropic Rearrangement and Applications in Total Synthesis of Sesquiterpenoids. , 2021, Journal of the American Chemical Society.

[2]  Chao Shen,et al.  Palladium-Catalyzed Asymmetric Hydroesterification of α-Aryl Acrylic Acids to Chiral Substituted Succinates. , 2021, Organic letters.

[3]  C. Tung,et al.  Direct 1,2-Dicarbonylation of Alkenes towards 1,4-Diketones via Photoredox Catalysis. , 2021, Angewandte Chemie.

[4]  Ruining Li,et al.  Synthesis of Unsymmetrical 1,4-Dicarbonyl Compounds by Photocatalytic Oxidative Radical Additions. , 2021, Organic letters.

[5]  S. Yadav,et al.  N ‐Heterocyclic Carbene (NHC)‐Catalyzed Intramolecular Stetter Reaction to Access Dibenzo‐fused Seven‐membered Heterocycles , 2021 .

[6]  C. Nevado,et al.  Asymmetric, visible light-mediated radical sulfinyl-Smiles rearrangement to access all-carbon quaternary stereocentres , 2021, Nature Chemistry.

[7]  Soumi Das,et al.  NHC-Catalyzed Desymmetrization of N-Aryl Maleimides Leading to the Atroposelective Synthesis of N-Aryl Succinimides. , 2021, Angewandte Chemie.

[8]  Qi Wu,et al.  Intramolecular Stereoselective Stetter Reaction Catalyzed by Benzaldehyde Lyase. , 2021, Angewandte Chemie.

[9]  Weiping Zhou,et al.  Gold(I)-Catalyzed Synthesis of Highly Substituted 1,4-Dicarbonyl Derivatives via Sulfonium [3,3]-Sigmatropic Rearrangement. , 2020, Organic letters.

[10]  M. Gravel,et al.  Enantioselective Stetter Reactions Catalyzed by Bis(amino)cyclopropenylidenes: Important Role for Water as an Additive. , 2020, Organic letters.

[11]  M. Heravi,et al.  Recent Advances in Stetter Reaction and Related Chemistry: An update , 2020 .

[12]  Z. Rafiński,et al.  N ‐Heterocyclic Carbene‐Catalyzed Enantioselective Intramolecular Annulations to Construct Benzo‐Fused Pyranones with Quaternary Stereocenter , 2020 .

[13]  P. Caboni,et al.  Tandem Wittig Reaction-Ring Contraction of Cyclobutanes: A Route to Functionalized Cyclopropanecarbaldehydes. , 2019, Organic letters.

[14]  G. Hilt,et al.  Electrochemical, Manganese-Assisted Carbon-Carbon Bond Formation between β-Keto Esters and Silyl Enol Ethers. , 2019, Organic letters.

[15]  C. Schindler,et al.  Total Syntheses of Herqulines B and C. , 2019, Journal of the American Chemical Society.

[16]  Shouyun Yu,et al.  Enantioselective Radical Hydroacylation of Enals with α-Ketoacids Enabled by Photoredox/Amine Cocatalysis. , 2019, Organic letters.

[17]  C. Mück‐Lichtenfeld,et al.  Bioinspired Radical Stetter Reaction: Radical Umpolung Enabled by Ion-Pair Photocatalysis. , 2019, Angewandte Chemie.

[18]  J. L. Wood,et al.  Total Synthesis of Herquline B and C. , 2019, Journal of the American Chemical Society.

[19]  Phil S Baran,et al.  Concise Total Synthesis of Herqulines B and C. , 2018, Journal of the American Chemical Society.

[20]  P. Melchiorre,et al.  Stereocontrolled Synthesis of 1,4‐Dicarbonyl Compounds by Photochemical Organocatalytic Acyl Radical Addition to Enals , 2018, Angewandte Chemie.

[21]  T. Donohoe,et al.  Synthesis of lamellarin alkaloids using orthoester-masked a -keto acids † , 2019 .

[22]  N. Maulide,et al.  A Catalytic Cross‐Olefination of Diazo Compounds with Sulfoxonium Ylides , 2018, Angewandte Chemie.

[23]  N. Maulide,et al.  Amide activation: an emerging tool for chemoselective synthesis. , 2018, Chemical Society reviews.

[24]  M. Gravel,et al.  Oxazolium Salts as Organocatalysts for the Umpolung of Aldehydes. , 2018, Organic letters.

[25]  D. Kaldre,et al.  Stereodivergent synthesis of 1,4-dicarbonyls by traceless charge–accelerated sulfonium rearrangement , 2018, Science.

[26]  Keshaba N. Parida,et al.  Cross-coupling of dissimilar ketone enolates via enolonium species to afford non-symmetrical 1,4-diketones , 2018, Beilstein journal of organic chemistry.

[27]  Z. Qian,et al.  Intermolecular Oxidative Radical Addition to Aromatic Aldehydes: Direct Access to 1,4- and 1,5-Diketones via Silver-Catalyzed Ring-Opening Acylation of Cyclopropanols and Cyclobutanols. , 2018, The Journal of organic chemistry.

[28]  R. J. Thomson,et al.  A Strategy for the Convergent and Stereoselective Assembly of Polycyclic Molecules. , 2018, Journal of the American Chemical Society.

[29]  I. Beletskaya,et al.  Stereodivergent Catalysis. , 2018, Chemical reviews.

[30]  N. Maulide,et al.  Chemoselective Intermolecular Cross-Enolate-Type Coupling of Amides , 2017, Journal of the American Chemical Society.

[31]  G. Evano,et al.  Keteniminium Ions: Unique and Versatile Reactive Intermediates for Chemical Synthesis , 2017, Synthesis.

[32]  Keshaba N. Parida,et al.  Enolonium Species-Umpoled Enolates. , 2017, Angewandte Chemie.

[33]  Phil S. Baran,et al.  11-Step Total Synthesis of (−)-Maoecrystal V , 2016, Journal of the American Chemical Society.

[34]  G. C. Fu,et al.  Enantioselective Decarboxylative Arylation of α-Amino Acids via the Merger of Photoredox and Nickel Catalysis. , 2016, Journal of the American Chemical Society.

[35]  S. Buchwald,et al.  Copper-catalyzed enantioselective stereodivergent synthesis of amino alcohols , 2016, Nature.

[36]  P. Bergmann Introduction To Strategies For Organic Synthesis , 2016 .

[37]  T. Hirao,et al.  Selective Intermolecular Oxidative Cross-Coupling of Enolates. , 2015, Journal of the American Chemical Society.

[38]  A. Biju,et al.  Recent Advances in the N-Heterocyclic Carbene (NHC)-Organocatalyzed Stetter Reaction and Related Chemistry , 2015, Synthesis.

[39]  Shenlin Huang,et al.  Catalytic asymmetric dearomatizing redox cross coupling of ketones with aryl hydrazines giving 1,4-diketones. , 2015, Journal of the American Chemical Society.

[40]  Rai‐Shung Liu,et al.  ZnII - and AuI-catalyzed regioselective hydrative oxidations of 3-en-1-ynes with Selectfluor: realization of 1,4-dioxo and 1,4-oxohydroxy functionalizations. , 2014, Chemistry.

[41]  Maria Teresa Oliveira,et al.  Dual catalysis becomes diastereodivergent. , 2013, Angewandte Chemie.

[42]  E. Carreira,et al.  Enantio- and Diastereodivergent Dual Catalysis: α-Allylation of Branched Aldehydes , 2013, Science.

[43]  A. Fürstner,et al.  Total synthesis of amphidinolide F. , 2006, Angewandte Chemie.

[44]  Maria Teresa Oliveira,et al.  Diastereodivergent de-epimerization in catalytic asymmetric allylic alkylation. , 2012, Angewandte Chemie.

[45]  J. Cochrane,et al.  Total synthesis of mycocyclosin. , 2012, Organic letters.

[46]  Xueliang Huang,et al.  Charge-Accelerated Sulfonium [3,3]-Sigmatropic Rearrangements , 2012 .

[47]  Maria Teresa Oliveira,et al.  Catalytic asymmetric diastereodivergent deracemization. , 2011, Angewandte Chemie.

[48]  A. Urakawa,et al.  Diastereodivergent asymmetric sulfa-Michael additions of α-branched enones using a single chiral organic catalyst. , 2011, Journal of the American Chemical Society.

[49]  jin-quan yu,et al.  Pd(II)‐Catalyzed Carbonylation of C(sp3)—H Bonds: A New Entry to 1,4‐Dicarbonyl Compounds. , 2011 .

[50]  J. Autschbach,et al.  Rhodium(II)-catalyzed cross-coupling of diazo compounds. , 2011, Angewandte Chemie.

[51]  jin-quan yu,et al.  Pd(II)-catalyzed carbonylation of C(sp3)-H bonds: a new entry to 1,4-dicarbonyl compounds. , 2010, Journal of the American Chemical Society.

[52]  H. Yorimitsu,et al.  Reaction of 2-(2,2,2-trifluoroethylidene)-1,3-dithiane 1-oxide with ketones under Pummerer conditions and its application to the synthesis of 3-trifluoromethyl-substituted five-membered heteroarenes. , 2010, Angewandte Chemie.

[53]  C. Ugwu,et al.  Biodegradability of Plastics , 2009, International journal of molecular sciences.

[54]  P. Baran,et al.  Intermolecular enolate heterocoupling: scope, mechanism, and application. , 2008, Journal of the American Chemical Society.

[55]  T. Rovis,et al.  Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes. , 2008, The Journal of organic chemistry.

[56]  R. J. Thomson,et al.  Oxidative carbon-carbon bond formation via silyl bis-enol ethers: controlled cross-coupling for the synthesis of quaternary centers. , 2007, Organic letters.

[57]  Yong Huang,et al.  Enantioselective organo-cascade catalysis. , 2005, Journal of the American Chemical Society.

[58]  F. Glorius,et al.  Organocatalyzed conjugate umpolung of α,β-unsaturated aldehydes for the synthesis of γ-butyrolactones , 2004 .

[59]  J. Bode,et al.  N-heterocyclic carbene-catalyzed generation of homoenolates: gamma-butyrolactones by direct annulations of enals and aldehydes. , 2004, Journal of the American Chemical Society.

[60]  J. Yasuda,et al.  Highly water-soluble matrix metalloproteinases inhibitors and their effects in a rat adjuvant-induced arthritis model. , 2002, Bioorganic & medicinal chemistry.

[61]  D. Enders,et al.  The First Asymmetric Intramolecular Stetter Reaction. , 1997 .

[62]  D. Enders,et al.  The First Asymmetric Intramolecular Stetter Reaction. Preliminary Communication , 1996 .

[63]  B. Herradón,et al.  The Claisen-Johnson Rearrangement Route to 1,4-Dicarbonyl Compounds: Synthesis of Ethyl 4-Ethoxy-4-alkenoates as Masked 4-Oxo Esters , 1992 .

[64]  T. Hudlický,et al.  Claisen/Ozonolysis Alternative to Alkylation of Enolate Anions. Synthesis of 1,4-Dicarbonyl Compounds , 1986 .

[65]  K. Johnson An Update. , 1984, Journal of food protection.

[66]  B. Giese,et al.  Steric Effects in the Addition of Alkyl Radicals to Alkenes , 1981 .

[67]  D. Evans,et al.  Enantioselective aldol condensations. 2. Erythro-selective chiral aldol condensations via boron enolates , 1981 .

[68]  D. Seebach,et al.  Methods of Reactivity Umpolung , 1979 .

[69]  H. Stetter Catalyzed Addition of Aldehydes to Activated Double Bonds—A New Synthetic Approach , 1976 .

[70]  H. Stetter,et al.  A New Method for Addition of Aldehydes to Activated Double Bonds , 1973 .

[71]  E. Corey,et al.  Synthesis of 1,n‐Dicarbonyl Derivates Using Carbanions from 1,3‐Dithianes , 1965 .

[72]  G. Gribble,et al.  Progress in the Chemistry of Organic Natural Products , 2011 .