期刊
JOURNAL OF NATURAL PRODUCTS
卷 64, 期 4, 页码 406-410出版社
AMER CHEMICAL SOC
DOI: 10.1021/np000550a
关键词
-
Several key reactions involving intramolecular cyclization, Grignard reaction, and ionic hydrogenation have been employed in a formal synthesis of sativene. The synthesis affords 3-isopropyl-6-methyltricyclo-[4.4.0.0(2,8)]decan-7-one, 12, McMurry's penultimate precursor to sativene, in 28% overall yield in eight steps starting with the commercially available racemic Wieland-Miescher ketone.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据