Towards the synthesis of HIV-protease inhibitors. Synthesis optically pure 3-carboxyl-decahydroisoquinolines.
摘要:
The synthesis of optically pure decahydroisoquinoline 1, a component of HIV-protease inhibitors, was accomplished in 30-33% overall yield from the readily available optically pure monoacid 4.
Towards the synthesis of HIV-protease inhibitors. Synthesis optically pure 3-carboxyl-decahydroisoquinolines.
作者:Ioannis N. Houpis、Audrey Molina、Robert A. Reamer、Joseph E. Lynch、R.P. Volante、Paul J. Reider
DOI:10.1016/s0040-4039(00)77633-7
日期:1993.4
The synthesis of optically pure decahydroisoquinoline 1, a component of HIV-protease inhibitors, was accomplished in 30-33% overall yield from the readily available optically pure monoacid 4.
Intermediates useful in the synthesis of HIV-protease inhibitors and methods for preparing the same
申请人:Albizati Francis Kim
公开号:US20050250949A1
公开(公告)日:2005-11-10
Optically active 3-amino-butene and 1,2-dihydroxy-3-amino-butane intermediate compounds, useful in the synthesis of HIV-protease inhibitors and methods of preparing these intermediate compounds are disclosed.