W. Doubleday

发表

Computer-assisted design and synthesis of novel aldose reductase inhibitors.

A. Treasurywala, J. Sredy, D. Loughney, 1989, Journal of medicinal chemistry.

The Process Development of Ravuconazole: An Efficient Multikilogram Scale Preparation of an Antifungal Agent(1)

J. Wasylak, S. Leung, Chien-Kuang Chen, 2009 .

Preparation of a Tricyclopropylamino Acid Derivative via Simmons–Smith Cyclopropanation with Downstream Intramolecular Aminoacetoxylation for Impurity Control

Y. Qiu, M. Hay, I. S. Young, 2016 .

A Practical Stereoselective Synthesis and Novel Cocrystallizations of an Amphiphatic SGLT-2 Inhibitor

S. Leung, R. Randazzo, K. Volk, 2012 .

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 1. Evolution of Enabling Strategies

D. Erdemir, Saravanababu Murugesan, R. J. Fox, 2017 .

Development of a Practical Synthesis of a p38 Kinase Inhibitor via a Safe and Robust Amination

S. Tummala, Paul C. Lobben, S. Leung, 2012 .

N-Amination of pyrrole and indole heterocycles with monochloramine (NH2Cl).

K. Leftheris, J. Hynes, A. Dyckman, 2004, The Journal of organic chemistry.

Allylcerium(III) compounds, powerful new synthetic reagents: a new stereocontrolled approach to olefins and methylene-interrupted polyenes

W. Doubleday, T. Cohen, Baoming Guo, 1987 .

Process research and development for a tetrazole-based growth hormone secretagogue (GHS) pharmaceutical development candidate.

M. Gleeson, R. L. Parsons, Zhongmin Xu, 2009, The Journal of organic chemistry.

Preparation and remarkable reactivity of the elusive (1,1,3,3-tetramethylallyl)lithium

W. Doubleday, Simon H. Yu, T. Cohen, 1992 .

A preparatively convenient ligand-free catalytic PEG 2000 Suzuki-Miyaura coupling.

Thomas M. Razler, Ruiling Fu, R. Khan, 2009, The Journal of organic chemistry.

Reaction of Allylmanganese(II) Reagents with Aldehydes

W. Doubleday, T. Cohen, Y. Ahn, 1995 .

Approaches to the assembly of the antifungal agent FR-900848: studies on the asymmetric synthesis of bicyclopropanes and an X-ray crystallographic analysis of (4R,5R)-2-[(1R,3S,4S,6R)-6-phenyl-1-bicyclopropyl]-1,3-dimethyl-4,5-diphenylimidazolidine

David J. Williams, A. Barrett, A. White, 1994 .

Total synthesis of antifungal natural products.

A. Barrett, D. Williams, P. Procopiou, 2000, Ernst Schering Research Foundation workshop.

ASSEMBLY OF THE ANTIFUNGAL AGENT FR-900848 AND THE CETP INHIBITOR U-106305: STUDIES ON REMARKABLE MULTICYCLOPROPANE NATURAL PRODUCTS

David J. Williams, A. Barrett, A. White, 1997 .

Asymmetric synthesis of bicyclopropane derivatives

A. Barrett, G. Tustin, W. Doubleday, 1996 .

Synthese asymetrique de beta-aminoacides chiraux

P. Colson, J. Behling, Carl M. Knable, 1997 .

Stereochemical elucidation of the pentacyclopropane antifungal agent FR-900848

A. Barrett, G. Tustin, W. Doubleday, 1996 .

PROCESS FOR THE PREPARATION OF GLUCURONIDE DRUG-LINKERS AND INTERMEDIATES THEREOF

A. Choudhury, P. Moquist, W. Doubleday, 2018 .

Preparation of the HIV Attachment Inhibitor BMS-663068. Part 9. Active Pharmaceutical Ingredient Process Development and Powder Properties

Richard L. Schild, Yande Huang, Antonio Ramirez, 2017 .

Practical Enantioselective Synthesis of β-Substituted-β-amino Esters

P. Colson, A. Awasthi, J. Duran, 2005 .