手性选择性合成 laurenditerpenol 的途径。
Enantioselective pathway for the synthesis of laurenditerpenol.
机构信息
Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138, USA.
出版信息
Org Lett. 2010 Apr 16;12(8):1836-8. doi: 10.1021/ol1004802.
PMID:20337419
Abstract
Simple enantioselective routes to the two key intermediates shown above (at center) for the synthesis of laurenditerpenol have been developed using a Diels-Alder step and the same catalyst system for each.
摘要
已经开发出了使用 Diels-Alder 步骤和相同的催化剂体系来合成上述（中间）laurenditerpenol 的两个关键中间体的简单对映选择性路线。
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