D. Krishnamurthy

发表

Catalytic Enantioselective Synthesis of Dihydropyrones via Formal Hetero Diels-Alder Reactions of "Danishefsky's Diene" with Aldehydes

G. E. Keck, Xiang Li, D. Krishnamurthy, 1995 .

PRONOUNCED SOLVENT AND CONCENTRATION EFFECTS IN AN ENANTIOSELECTIVE MUKAIYAMA ALDOL CONDENSATION USING BINOL-TITANIUM(IV) CATALYSTS

G. E. Keck, D. Krishnamurthy, 1995 .

Noncryogenic I/Br-Mg exchange of aromatic halides bearing sensitive functional groups using i-PrMgCl-bis[2-(N,N-dimethylamino)ethyl] ether complexes.

C. Senanayake, Xiaojun Wang, L. Zhang, 2006, Organic letters.

9.3 Industrial Applications of Asymmetric Synthesis: Asymmetric Synthesis as an Enabler of Green Chemistry

Jinhua J. Song, C. Senanayake, D. Krishnamurthy, 2012 .

Asymmetric Oxidation of a Dihydrothienopyrimidine

C. Senanayake, N. Grinberg, N. Haddad, 2017 .

Practical and Highly Stereoselective Technology for Preparation of Enantiopure Sulfoxides and Sulfinamides Utilizing Activated and Functionally Differentiated N‐Sulfonyl‐1,2,3‐oxathiazolidine‐2‐oxide Derivatives.

C. Senanayake, Zhi-Hui Lu, Z. Han, 2005 .

Palladium-catalyzed coupling of vinyl tosylates with arylsulfinate salts

C. Senanayake, Heewon Lee, N. Haddad, 2009 .

Oxaphosphole-Based Monophosphorus Ligands for Palladium-Catalyzed Amination Reactions

C. Senanayake, Heewon Lee, B. Qu, 2011 .

A general and special catalyst for Suzuki-Miyaura coupling processes.

C. Senanayake, A. White, Xudong Wei, 2010, Angewandte Chemie.

Mild iodine-magnesium exchange of iodoaromatics bearing a pyrimidine ring with isopropylmagnesium chloride.

C. Senanayake, Xiaojun Wang, L. Zhang, 2006, Organic letters.

Synthesis of potent lymphocyte function‐associated antigen‐1 inhibitors labeled with carbon‐14 and deuterium, part 1

C. Senanayake, Denis Byrne, L. Nummy, 2011 .

cis-1-Amino-2-Indanol-Derived Ligands in Asymmetric Catalysis

I. Gallou, C. Senanayake, D. Krishnamurthy, 2005 .

Practical Synthesis of A Benzophenone-Based NNRT Inhibitor of HIV-1

C. Yoakim, Jeff O'meara, S. Landry, 2012 .

Novel, tunable, and efficient chiral bisdihydrobenzooxaphosphole ligands for asymmetric hydrogenation.

C. Senanayake, Xudong Wei, N. Yee, 2010, Organic letters.

An improved method of amide synthesis using acyl chlorides

J. Wang, C. Senanayake, N. Grinberg, 2009 .

Convenient Preparation of Chiral Primary Alcohols via Catalytic Asymmetric Reduction of Aldehydes Using Bu(3)SnD.

G. E. Keck, D. Krishnamurthy, 1996, The Journal of organic chemistry.

Chelation controlled reductive amination of cyclic ketones to trans-4-methoxycyclohexylamines: 9-BBN reduction mediated with FeCl3

C. Senanayake, Shengli Ma, Heewon Lee, 2012 .

Addition of grignard reagents to aryl acid chlorides: an efficient synthesis of aryl ketones.

C. Senanayake, Xiaojun Wang, L. Zhang, 2005, Organic letters.

A Simple and Practical Synthesis of (+)-2-Bromobicyclo[2.2.1]hept-5-ene-2-carboxaldehyde via Chiral Lewis Acid Catalyzed [4+2] Cycloaddition

G. E. Keck, D. Krishnamurthy, 1996 .

Expedient synthesis of substituted imidazoles from nitriles

I. Gallou, C. Senanayake, D. Krishnamurthy, 2005 .

Palladium catalyzed alkoxy- and aminocarbonylation of vinyl tosylates.

C. Senanayake, Heewon Lee, N. Haddad, 2011, Organic letters.

Palladium-catalyzed aminocarbonylation of heteroaryl halides using di-tert-butylphosphinoferrocene

C. Senanayake, Heewon Lee, N. Grinberg, 2009 .

Novel and efficient chiral bisphosphorus ligands for rhodium-catalyzed asymmetric hydrogenation.

C. Senanayake, A. White, Xudong Wei, 2010, Organic letters.

3.18 Synthetically Derived Auxiliaries: Sulfur Derivatives (including Sulfilamines and Sulfoximines)

C. Senanayake, Z. Han, D. Krishnamurthy, 2012 .

First application of tunable alkyl or aryl sulfinamides to the stereoselective synthesis of a chiral amine: asymmetric synthesis of (R)-didesmethylsibutramine ((R)-DDMS) using (R)-triethylmethylsulfinamide ((R)-TESA).

C. Senanayake, Z. Han, D. Krishnamurthy, 2002, Organic letters.

Properly designed modular asymmetric synthesis for enantiopure sulfinamide auxiliaries from N-sulfonyl-1,2,3-oxathiazolidine-2-oxide agents.

C. Senanayake, Z. Han, D. Krishnamurthy, 2002, Journal of the American Chemical Society.

Asymmetric synthesis of cetirizine dihydrochloride

C. Senanayake, Z. Han, D. Krishnamurthy, 2002 .

Catalytic asymmetric allylation reactions. 3. Extension to methallylstannane, comparison of procedures, and observation of a nonlinear effect

M. Grier, G. E. Keck, D. Krishnamurthy, 1993 .

A practical synthesis of 2-(N-substituted)-aminobenzimidazoles utilizing CuCl-promoted intramolecular cyclization of N-(2-aminoaryl)thioureas

C. Senanayake, Xiaojun Wang, L. Zhang, 2004 .

Synthetic studies on the rhizoxins. 1. Two stereoselective routes to a functionalized C(1)-C(9) subunit

G. E. Keck, D. Krishnamurthy, Minnie Park, 1993 .

The Role and Importance of cis-1-Amino-2-Indanol in Biological Systems and Asymmetric Processes

I. Gallou, C. Senanayake, D. Krishnamurthy, 2005 .

Development of a Scalable Process for 1-(3,5-Dichlorophenyl)-5-iodo-3-methyl- (4-methylbenzyl)-1H-imidazo[1,2-a]imidazol-2-one: A Key Intermediate for the Synthesis of LFA-1 Inhibitors

Michael D. Johnson, C. Senanayake, Denis Byrne, 2005 .

A practical synthesis of LFA-1 inhibitors utilizing CuCl-promoted intramolecular cyclization of thiohydantoins

C. Senanayake, S. Shen, Denis Byrne, 2005 .

Asymmetric synthesis of homopropargylic alcohols from aldehydes and allenyltri-n-butylstannane

Xiaoming Chen, G. E. Keck, D. Krishnamurthy, 1994 .

Efficient asymmetric synthesis of P-chiral phosphine oxides via properly designed and activated benzoxazaphosphinine-2-oxide agents.

Jinhua J. Song, C. Senanayake, Shengli Ma, 2013, Journal of the American Chemical Society.

Synthesis of a highly potent leukocyte function-associated antigen-1 antagonist and its metabolite labeled with stable isotopes and carbon-14, part 2

C. Senanayake, B. Latli, D. Krishnamurthy, 2011 .

A new and practical boronic acid catalyzed intramolecular cyclodehydration of ureas for the synthesis of LFA-1 antagonists

C. Senanayake, J. Mulder, Xiaojun Wang, 2011 .

Synthesis of labeled ambroxol and its major metabolites

C. Senanayake, B. Latli, D. Retz, 2009 .

Asymmetric synthesis of diverse α,α-diarylmethylamines via aryl Grignard additions to chiral N-2,4,6-triisopropylbenzenesulfinylimines

C. Senanayake, K. Fandrick, Z. Han, 2011 .

Design and synthesis of chiral oxathiozinone scaffolds: efficient synthesis of hindered enantiopure sulfinamides and sulfinyl ketimines.

Jinhua J. Song, C. Senanayake, Shengli Ma, 2013, Angewandte Chemie.

Enantioselective synthesis of diverse sulfinamides and sulfinylferrocenes from phenylglycine-derived chiral sulfinyl transfer agent.

C. Senanayake, N. Grinberg, B. Lu, 2011, The Journal of organic chemistry.

Facile entry to an efficient and practical enantioselective synthesis of a polycyclic cholesteryl ester transfer protein inhibitor.

Jinhua J. Song, M. Ostermeier, J. Mack, 2014, Organic letters.

Efficient synthesis of Empagliflozin, an inhibitor of SGLT-2, utilizing an AlCl3-promoted silane reduction of a β-glycopyranoside.

C. Senanayake, N. Yee, D. Weber, 2014, Organic letters.

Synthesis of [14C]-, [13C4]-, and [13C4,15N2]- 5-amino-4-iodopyrimidine

C. Senanayake, B. Latli, Paul-James Jones, 2008 .

Bis[2‐(N,N‐dimethylamino)ethyl] Ether

C. Senanayake, Xiaojun Wang, L. Zhang, 2011 .

Catalytic asymmetric hydrogenation of heterocyclic ketone-derived hydrazones, pronounced solvent effect on the inversion of configuration

C. Senanayake, Shengli Ma, Heewon Lee, 2011 .

Palladium-catalyzed cross-coupling of cyclopropylmagnesium bromide with aryl bromides mediated by zinc halide additives.

C. Senanayake, Xiaojun Wang, L. Zhang, 2010, The Journal of organic chemistry.

New resolution approach for large-scale preparation of enantiopure didesmethylsibutramine (DDMS)

C. Senanayake, Z. Han, D. Krishnamurthy, 2003 .

Chemical synthesis of allyl-[13C6]-glucuronate

C. Senanayake, B. Latli, D. Krishnamurthy, 2011 .

Asymmetric Total Synthesis of Rhizoxin D.

K. Savin, Travis T Wager, John Covel, 2001, Angewandte Chemie.

Development of a preparative-scale asymmetric synthesis of (R)-p-tolyl methyl sulfoxide for use in a one-pot synthesis of a drug intermediate containing a trifluoromethyl-substituted alcohol functionality

Jinhua J. Song, C. Senanayake, N. Yee, 2007 .

Synthesis of [14C] ‐ and [13C6]‐labeled tipranavir and its potential hydroxyl metabolite and the glucuronide conjugate

C. Senanayake, B. Latli, D. Krishnamurthy, 2008 .

Catalytic Asymmetric Allylation Reactions:(S)‐1‐(Phenylmethoxy)‐4‐Penten‐2‐ol

G. E. Keck, D. Krishnamurthy, 2003 .

Synthesis of [14C]-and [13C6]-labeled potent HIV non-nucleoside reverse transcriptase inhibitor

C. Senanayake, B. Latli, C. Busacca, 2009 .

First practical synthesis of enantiomerically pure (R)- and (S)-desmethylsibutramine (DMS) and unambiguous determination of their absolute configuration by single-crystal X-ray analysis

C. Senanayake, Z. Han, D. Krishnamurthy, 2002 .

Synthesis of tritium‐labeled bilirubin

C. Senanayake, B. Latli, D. Krishnamurthy, 2008 .

General solution to the synthesis of N-2-substituted 1,2,3-triazoles.

P. Wipf, C. Senanayake, Xiaojun Wang, 2010, Organic letters.

Bromo-directed N-2 alkylation of NH-1,2,3-triazoles: efficient synthesis of poly-substituted 1,2,3-triazoles.

C. Senanayake, N. Haddad, Xiaojun Wang, 2009, Organic letters.

Highly regioselective N-2 arylation of 4,5-dibromo-1,2,3-triazole: efficient synthesis of 2-aryltriazoles.

C. Senanayake, Heewon Lee, N. Haddad, 2009, Organic letters.

An efficient synthesis of [13C6]-3,5-dichloroaniline

C. Senanayake, B. Latli, D. Krishnamurthy, 2008 .

Pronounced Solvent and Concentration Effects in an Enantioselective Mukaiyama Aldol Condensation Using BINOL‐Titanium(IV) Catalysts.

G. E. Keck, D. Krishnamurthy, 1995 .

Oxaphosphole‐Based Monophosphorus Ligands for Palladium‐Catalyzed Amination Reactions.

C. Senanayake, Heewon Lee, B. Qu, 2011 .

Heart-Cutting Two-Dimensional Ultrahigh-Pressure Liquid Chromatography for Process Development: Asymmetric Reaction Monitoring

Jinhua J. Song, C. Senanayake, Shaun Mendonsa, 2013 .

A highly selective and practical method for enantiopure sulfoxides utilizing activated and functionally differentiated N-sulfonyl-1,2,3-oxathiazolidine-2-oxide derivatives.

C. Senanayake, Zhi-Hui Lu, Z. Han, 2003, Angewandte Chemie.