Studies on Agarofurans Ⅱ.Stereoselective Synthesis of 1α-and 1β-Methyl Agarofuran

作     者：Wu Yan ZHANG Ji Yu GUO Xiao Tian LIANG (Insitute of Materia Medica, Chinese Academy of Med. Sci. & Peking Union Med. College, Beijing 100050) 

作者机构：Institute of Materia Medica Chinese Academy of Med. Sci. Peking Union Med. College Beijing 100050 China 

出 版 物：《Chinese Chemical Letters》 (中国化学快报（英文版）)

年 卷 期：1997年第8卷第6期

页      面：491-492页

核心收录：

学科分类：081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070303[理学-有机化学] 0703[理学-化学] 

主　　题：and 1 Stereoselective Synthesis of 1 Studies on Agarofurans Methyl Agarofuran 

摘      要：1α- and 1β-methyl agarofuran 1 and 2 were stereoselectively synthesized. the key intermediates being synthesized through stereoselective Robinson *** conjugated double bond was redined in an improved way. Alkylation of imine 7 with enone 8, 9, 10 was performed