CuI /反-4-羟基-1-脯氨酸催化的芳基碘化物与叔丁基β-酮酯的偶联在DMF中在40°C下顺利进行,在酸促进叔丁酯的脱保护和脱羧反应后得到α-芳基酮团体。CuI / 2-吡啶甲酸在二恶烷中于70°C催化芳基碘化物与乙酰乙酸叔丁酯偶合时,在自发脱酰作用下释放出α-芳酸叔丁酯。各种各样的官能团,例如乙酰基,甲氧基,腈,硝基,溴和氯与反应条件相容。
Novel peptides as NS3-serine protease inhibitors of hepatitis C virus
申请人:Saksena K. Anil
公开号:US20070032433A1
公开(公告)日:2007-02-08
The present invention discloses novel compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such compounds as well as methods of using them to treat disorders associated with the HCV protease.
NOVEL PEPTIDES AS NS3-SERINE PROTEASE INHIBITORS OF HEPATITIS C VIRUS
申请人:Saksena Anil K.
公开号:US20110117057A1
公开(公告)日:2011-05-19
The present invention discloses novel compounds which have HCV protease inhibitory activity as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising such compounds as well as methods of using them to treat disorders associated with the HCV protease.