P. Dagneau

发表

A catalytic asymmetric three-component 1,4-addition/aldol reaction: enantioselective synthesis of the spirocyclic system of vannusal A.

Raffaella Faraoni, K. Nicolaou, Wenjun Tang, 2005, Angewandte Chemie.

Synthesis of antifungal glucan synthase inhibitors from enfumafungin.

Shane W. Krska, R. Ball, M. McLaughlin, 2012, The Journal of organic chemistry.

Total synthesis of the originally assigned structure of vannusal B.

K. Nicolaou, A. Ortiz, Hongjun Zhang, 2008, Angewandte Chemie.

Total synthesis and structural revision of vannusals A and B: synthesis of the originally assigned structure of vannusal B.

Raffaella Faraoni, K. Nicolaou, M. Jennings, 2010, Journal of the American Chemical Society.

Practical asymmetric synthesis of a potent PDE4 inhibitor via stereoselective enolate alkylation of a chiral aryl-heteroaryl secondary tosylate.

L. Tan, E. Grabowski, Cheng-yi Chen, 2005, The Journal of organic chemistry.

Practical enantioselective synthesis of a COX-2 specific inhibitor

L. Tan, P. Reider, E. Grabowski, 2002 .

An efficient synthesis of the natural (+)-fulvanin 1

P. Dagneau, P. Canonne, 1996 .

An expedient entry into the fused polycyclic skeleton of vannusal AElectronic supplementary information (ESI) available: selected physical data for compounds 11 and 2. See http://www.rsc.org/suppdata/cc/b2/b208234a/Dedicated to Professor Herbert C. Brown on the occasion of his 90th birthday.

K. Nicolaou, M. Jennings, P. Dagneau, 2002 .

Practical asymmetric synthesis of a potent Cathepsin K inhibitor. Efficient palladium removal following Suzuki coupling.

P. Prasit, R. Oballa, E. Grabowski, 2003, The Journal of organic chemistry.