Enantioselective Total Synthesis of Four Styrylpyrone Derivatives
Enantioselective Total Synthesis of Four Styrylpyrone Derivatives作者机构:Department of Chemistry&National Laboratory of Applied Organic ChemistryLanzhou UniversityLanzhou 730000
出 版 物:《Chinese Chemical Letters》 (中国化学快报(英文版))
年 卷 期:2002年第13卷第6期
页 面:519-520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]
基 金:We are grateful to the National Natural Science Foundation of China(No.2017223)for financial support
主 题:Enantioselective 5-acetoxygoniothalamin 5-acetoxyisogoniothalamin oxide 6R-(+)- goniothalamin (6R, 7R, 8R)-(+)-goniothalamin oxide.
摘 要:The first enantioselective total synthesis of 5-acetoxygoniothalamin 1 and 5-acetoxyisogoniothalamin oxide 2 was achieved through the Sharpless kinetic resolution of racemic secondary 2- furylmethanol 5 and the Mitsunobu reaction. At the same time we developed a short synthetic route for 6R-(+)-goniothalamin 3 and (6R, 7R, 8R)-(+)-goniothalamin oxide 4. And according to this route the configuration of 5-acetoxygoniothalamin 1 was confirmed as (5S, 6S).