Joseph K. Barbay, Ph.D.

2002 Harvard University, Cambridge, MA, United States 
synthesis of natural products
"Joseph Barbay"
Mean distance: 8.28


Sign in to add mentor
Andrew G. Myers grad student 2002 Harvard
 (Asymmetric synthesis of monofluorinated analogs of the Merck HIV protease inhibitor indinavir.)
BETA: Related publications


You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...