Lipase-mediated diastereoselective and enantioselective acetylations of 3-substituted cyclohexanols
摘要:
Lipase-mediated acetylation of four diastereomeric and enatiomeric isomers of 3-substituted cyclohexanols 2 has led to an efficient resolution to provide a single stereoisomer, (1R,3S)-cyclohexyl acetate (1R,3S)-3 in a high enantiomeric excess. (C) 1998 Elsevier Science Ltd. All rights reserved.
PYRIMIDINONE CARBOXAMIDE INHIBITORS OF ENDOTHELIAL LIPASE
申请人:BRISTOL-MYERS SQUIBB COMPANY
公开号:US20150065505A1
公开(公告)日:2015-03-05
The present invention provides compounds of Formula (I), as defined in the specification and compositions comprising any of such novel compounds. These compounds are endothelial lipase inhibitors which may be used as medicaments.
Lipase-mediated diastereoselective and enantioselective acetylations of 3-substituted cyclohexanols
作者:Rikuhei Tanikaga、Akira Morita
DOI:10.1016/s0040-4039(97)10705-5
日期:1998.2
Lipase-mediated acetylation of four diastereomeric and enatiomeric isomers of 3-substituted cyclohexanols 2 has led to an efficient resolution to provide a single stereoisomer, (1R,3S)-cyclohexyl acetate (1R,3S)-3 in a high enantiomeric excess. (C) 1998 Elsevier Science Ltd. All rights reserved.