Joseph K. Barbay, Ph.D.

Affiliations: 
2002 Harvard University, Cambridge, MA, United States 
Area:
synthesis of natural products
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Andrew G. Myers grad student 2002 Harvard
 (Asymmetric synthesis of monofluorinated analogs of the Merck HIV protease inhibitor indinavir.)
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Publications

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MYERS AG, MCKINSTRY L, BARBAY JK, et al. (2010) ChemInform Abstract: Practical Methodology for the Asymmetric Synthesis of Organofluorine Compounds. Cheminform. 29: no-no
Xing C, LaPorte JR, Barbay JK, et al. (2004) Identification of GAPDH as a protein target of the saframycin antiproliferative agents. Proceedings of the National Academy of Sciences of the United States of America. 101: 5862-6
Myers AG, Barbay JK, Zhong B. (2001) Asymmetric synthesis of chiral organofluorine compounds: use of nonracemic fluoroiodoacetic acid as a practical electrophile and its application to the synthesis of monofluoro hydroxyethylene dipeptide isosteres within a novel series of HIV protease inhibitors. Journal of the American Chemical Society. 123: 7207-19
Myers AG, Barbay JK. (2001) On the inherent instability of alpha-amino alpha'-fluoro ketones. Evidence for their transformation to reactive oxyvinyliminium ion intermediates. Organic Letters. 3: 425-8
Myers AG, McKinstry L, Barbay JK, et al. (1998) Practical methodology for the asymmetric synthesis of organofluorine compounds Tetrahedron Letters. 39: 1335-1338
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