J. Studley

发表

Strategies for the modulation of phase II metabolism in a series of PKCε inhibitors.

R. Heim, J. Abt, A. Termin, 2014, Bioorganic & medicinal chemistry letters.

Sulfur Ylide-Mediated Catalytic Asymmetric Epoxidation and Aziridination

R. Fieldhouse, V. Aggarwal, A. Thompson, 1999 .

Studies of the zinc(II) catalysed addition of silyl enol ethers to cyclic enol ethers

M. Wills, J. Studley, 1993 .

Synthesis and evaluation of novel prodrugs of caspase inhibitors.

P. Weber, J. Charrier, J. Studley, 2012, Bioorganic & medicinal chemistry letters.

The discovery of the potent aurora inhibitor MK-0457 (VX-680).

David Bebbington, Michael O'Donnell, Damien Fraysse, 2009, Bioorganic & medicinal chemistry letters.

Novel catalysts for asymmetric reduction of carbonyl groups

M. Wills, Mark P. Gamble, J. Studley, 1999 .

DESIGN, SYNTHESIS AND APPLICATIONS OF A KETONE REDUCTION CATALYST CONTAINING A PHOSPHINAMIDE COMBINED WITH A DIOXABOROLIDINE UNIT

M. Wills, Mark P. Gamble, J. Studley, 1996 .

New catalysts containing an N-PO structural unit for the asymmetric reduction of ketones.

M. Wills, J. Studley, B. Burns, 1993 .

PHOSPHINAMIDES CATALYSTS CONTAINING A STEREOGENIC PHOSPHORUS ATOM FOR THE ASYMMETRIC REDUCTION OF KETONES BY BORANE

N. Alcock, M. Wills, Mark P. Gamble, 1997 .

Chiral phosphinamides: new catalysts for the asymmetric reduction of ketones by borane

Heather Tye, M. Wills, N. King, 1998 .

New chiral phosphinamide catalysts for highly enantioselective reduction of ketones

M. Wills, Mark P. Gamble, J. Studley, 1996 .

Stereoelectronic requirements for a new class of asymmetric ketone reduction catalysts containing an NPO structural unit.

Heather Tye, M. Wills, N. King, 1994 .

Catalytic Asymmetric Synthesis of Epoxides from Aldehydes Using Sulfur Ylides with In Situ Generation of Diazocompounds.

G. Hynd, M. Porcelloni, V. Aggarwal, 2001, Angewandte Chemie.

A new protocol for the in situ generation of aromatic, heteroaromatic, and unsaturated diazo compounds and its application in catalytic and asymmetric epoxidation of carbonyl compounds. Extensive studies to map out scope and limitations, and rationalization of diastereo- and enantioselectivities.

G. Hynd, M. Porcelloni, V. Aggarwal, 2003, Journal of the American Chemical Society.

Synthesis of epoxides from aldehydes and tosylhydrazone salts catalysed by triphenylarsine: complete trans selectivity for all combinations of coupling partners.

V. Aggarwal, J. Studley, Mamta Patel, 2002, Chemical communications.

The use of phosphinamide N-protecting groups in the diastereoselective reduction of ketones

M. Wills, J. Studley, M. Palmer, 1997 .

Design, Synthesis and Applications of a Ketone Reduction Catalyst Containing a Phosphinamide Combined with a Dioxaborolidine Unit.

M. Wills, Mark P. Gamble, J. Studley, 1997 .

New Catalysts Containing an N-P=O Structural Unit for the Asymmetric Reduction of Ketones.

M. Wills, J. Studley, B. Burns, 1994 .

Toward ideality: the synthesis of (+)-kalkitoxin and (+)-hydroxyphthioceranic acid by assembly-line synthesis.

Matthew Burns, V. Aggarwal, Teerawut Bootwicha, 2015, Journal of the American Chemical Society.

Phosphinamides Catalysts Containing a Stereogenic Phosphorus Atom for the Asymmetric Reduction of Ketones by Borane.

N. Alcock, M. Wills, Mark P. Gamble, 1997 .

The discovery of the potent aurora inhibitor MK-0457 (VX-680).

M. Mortimore, D. Kay, D. Bebbington, 2009, Bioorganic & medicinal chemistry letters.