A. Choy

发表

Synthesis and SAR of novel conformationally-restricted oxazolidinones possessing gram-positive and fastidious gram-negative antibacterial activity. Part 1: Substituted pyrazoles.

Ji-Young Kim, M. Huband, Xiujuan Wu, 2007, Bioorganic & medicinal chemistry letters.

Lab on a Chip An “ occlusive thrombosis-on-a-chip ” microfluidic device for investigating the effect of antithrombotic drugs †

K. Kolaja, M. F. Peters, C. Pin, 2020 .

Developing in vitro assays to transform gastrointestinal safety assessment: potential for microphysiological systems.

Clay W Scott, K. Kolaja, M. F. Peters, 2020, Lab on a chip.

Deconvoluting Kinase Inhibitor Induced Cardiotoxicity

Godfrey L. Smith, Clay W Scott, Jonna C. Stålring, 2017, Toxicological sciences : an official journal of the Society of Toxicology.

Synthesis, Structure, and SAR of Tetrahydropyran-Based LpxC Inhibitors.

Matthew D. Miller, P. Ross, Michael R. Hale, 2014, ACS medicinal chemistry letters.

Solvent Effects on Diastereoselective Intramolecular [2 + 2] Photocycloadditions: Reversal of Selectivity through Intramolecular Hydrogen Bonding

M. Crimmins, A. Choy, 1997 .

Development of a Synthesis For a Long-Term Oxazolidinone Antibacterial

C. Huber, A. Choy, M. Pamment, 2008 .

An Improved Synthetic Preparation of 3-Butenal

M. Crimmins, S. Kirincich, A. Wells, 1998 .

Ring closing metathesis for the formation of medium ring ethers: the total synthesis of (−)-isolaurallene

M. Crimmins, A. Choy, K. Emmitte, 2002 .

Solvent Effects of Diastereoselective Intramolecular [2 + 2] Photocycloadditions: Reversal of Selectivity Through Intramolecular Hydrogen Bonding.

M. Crimmins, A. Choy, 1998 .

Approach to the homoerythrina alkaloids using a tandem N-alkylation/azomethine ylide cycloaddition.

J. Kampf, J. Kropf, W. H. Pearson, 2007, The Journal of organic chemistry.

Asymmetric Aldol-Ring-Closing Metathesis Strategy for the Enantioselective Construction of Six- to Nine-Membered Oxygen Heterocycles.

M. Crimmins, A. Choy, 1997, The Journal of organic chemistry.

Asymmetric Aldol—Ring-Closing Metathesis Strategy for the Enantioselective Construction of Six- to Nine-Membered Oxygen Heterocycles.

M. Crimmins, A. Choy, 1998 .

An Asymmetric Aldol—Ring‐Closing Metathesis Strategy for the Enantioselective Construction of Oxygen Heterocycles: An Efficient Approach to the Enantioselective Synthesis of (+)‐Laurencin.

M. Crimmins, A. Choy, 1999 .

Translating slow-binding inhibition kinetics into cellular and in vivo effects.

Peter J Tonge, Virna J A Schuck, Zhiping You, 2015, Nature chemical biology.

Human 3D Gastrointestinal Microtissue Barrier Function As a Predictor of Drug-Induced Diarrhea

Clay W Scott, M. F. Peters, T. Landry, 2018, Toxicological sciences : an official journal of the Society of Toxicology.

An Asymmetric Aldol−Ring-Closing Metathesis Strategy for the Enantioselective Construction of Oxygen Heterocycles: An Efficient Approach to the Enantioselective Synthesis of (+)-Laurencin

M. Crimmins, A. Choy, 1999 .

Antibacterial oxazolidinones possessing a novel C-5 side chain. (5R)-trans-3-[3-Fluoro-4- (1-oxotetrahydrothiopyran-4-yl)phenyl]-2- oxooxazolidine-5-carboxylic acid amide (PF-00422602), a new lead compound.

J. Brieland, Ji-Young Kim, M. Huband, 2007, Journal of medicinal chemistry.

An efficient, general asymmetric synthesis of carbocyclic nucleosides: application of an asymmetric aldol/ring-closing metathesis strategy.

W. Zuercher, B. W. King, M. Crimmins, 2000, The Journal of organic chemistry.

An Efficient, General Asymmetric Synthesis of Carbocyclic Nucleosides: Application of an Asymmetric Aldol/Ring‐Closing Metathesis Strategy.

W. Zuercher, B. W. King, M. Crimmins, 2001 .

Synthesis and structure-activity studies of novel homomorpholine oxazolidinone antibacterial agents.

Ji-Young Kim, M. Huband, F. E. Boyer, 2009, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of novel conformationally restricted oxazolidinones possessing gram-positive and fastidious gram-negative antibacterial activity. Part 2: Amino substitutions on heterocyclic D-ring system.

M. Huband, F. E. Boyer, J. V. Vara Prasad, 2007, Bioorganic & Medicinal Chemistry Letters.