P. Vayron

发表

Toward antibody-catalyzed hydrolysis of organophosphorus poisons.

P. Renard, J. Grassi, C. Mioskowski, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Method of preparing ester of 1,5-diphenylpyrazole carboxylic acid.

M. Daumas, P. Vayron, 2004 .

Design and Synthesis of an α,α‐Difluorophosphinate Hapten for Antibody‐Catalyzed Hydrolysis of Organophosphorus Nerve Agents

P. Renard, A. Valleix, C. Mioskowski, 2000 .

Easy access to phosphonothioates.

P. Renard, A. Valleix, C. Mioskowski, 2002, Chemistry.

Easy access to phosphonothioates.

P. Renard, A. Valleix, C. Mioskowski, 2002, Chemistry.

Optimized access to alkyl thiocyanates

P. Renard, E. Leclerc, C. Mioskowski, 2001 .

Asymmetric hydrogenation of trisubstituted N-acetyl enamides derived from 2-tetralones using ruthenium-SYNPHOS catalysts: a practical synthetic approach to the preparation of β3-adrenergic agonist SR58611A

T. Ayad, P. Vayron, C. Pautigny, 2010 .

Lewis acid catalyzed room-temperature Michaelis-Arbuzov rearrangement.

P. Renard, E. Leclerc, A. Valleix, 2003, Angewandte Chemie.

Looking forward: a glance into the future of organic chemistry

S. Py, N. Moitessier, F. Robert, 2006 .

Trimethylsilyl halide-promoted Michaelis-Arbuzov rearrangement.

P. Renard, C. Mioskowski, P. Vayron, 2003, Organic letters.

Method for preparation of sulfonamide derivatives-benzofuran

P. Vayron, Thomas Priem, 2010 .