Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bridgette Craig"'
Autor:
Perry Michael David, James Saenz, Kim Albizati, Sami Bahmanyar, Billie J. Kline, Mark A. Mitchell, Bridgette Craig-Woods, Nebojsa Stankovic, Shu Yu
Publikováno v:
Organic Process Research & Development. 11:30-38
A practical process for the synthesis of PPARγ agonist AG035029 was developed which involved six steps along the longest linear path. The process development utilized automated technology and compu...
Autor:
Ramon J. Alabaster, Roger N. Farr, Simon A Johnson, Guo-Jie Ho, John Y. L. Chung, Bridgette Craig, Andrew W. Gibson, Guy R. Humphrey, John S Edwards, Edward J. J. Grabowski
Publikováno v:
Tetrahedron: Asymmetry. 14:3503-3515
An efficient, high yield process for the synthesis of a GnRH antagonist has been developed. We have demonstrated that under boron trifluoride mediation, nosyl aziridines will react with 2-arylindole derivatives to afford β-substituted tryptamines in
Autor:
Jing Li, David J. Mathre, Joseph F. Payack, James M. McNamara, Nancy N. Tsou, David M. Tschaen, Karel M. J. Brands, Karl B. Hansen, Paul J. Reider, Bridgette Craig, Peter G. Dormer, Mark A. Huffman, Philip J. Pye, Todd D. Nelson, Kai Rossen, Robert A. Reamer, Alexander Candelario, Jonathan D. Rosen, Christopher J. Welch, Zhiguo J. Song, Paul N. Devine, Matthew M. Zhao
Publikováno v:
Journal of the American Chemical Society. 125:2129-2135
An efficient stereoselective synthesis of the orally active NK(1) receptor antagonist Aprepitant is described. A direct condensation of N-benzyl ethanolamine with glyoxylic acid yielded a 2-hydroxy-1,4-oxazin-3-one which was activated as the correspo
Autor:
Jacqueline H. Smitrovich, Mark A. Huffman, Joseph F. Payack, Louis Matty, Jonathan D. Rosen, James M. McNamara, Todd D. Nelson, Bridgette Craig
Publikováno v:
ChemInform. 36
Autor:
Mark A. Huffman, Todd D. Nelson, Jacqueline H. Smitrovich, James M. McNamara, Bridgette Craig, Joseph F. Payack, Louis Matty, Jonathan D. Rosen
Publikováno v:
Organic letters. 7(1)
The concise synthesis of a stereochemically rich hNK-1 receptor antagonist is described. The synthesis is highlighted by an S(N)2 reaction of an enantiomerically pure alpha-alkoxy sulfonate (orthogonally protected butane triol), which was prepared by
Autor:
James Saenz, Mark Mitchell, Sami Bahmanyar, Nebojsa Stankovic, Michael Perry, Bridgette Craig-Woods, Billie Kline, Shu Yu, Kim Albizati
Publikováno v:
Organic Process Research & Development; Jan2007, Vol. 11 Issue 1, p30-38, 9p