期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 130, 期 9, 页码 2783-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja7113757
关键词
-
资金
- NHLBI NIH HHS [HL25848] Funding Source: Medline
The Diels-Alder reactions between vinylindenes (5 or 6) as the dienes with quinoneketals (7 or 8) or with methacrolein as the dienophiles were investigated. The remarkable regioselectivities of these Diels-Alder adducts suggested that the regiopreferences of these dienes and dienophiles in these cases are not a fixed property of each component of the cycloaddition but are mutually contigent. This paper shows how the Diels-Alder reaction between 6 and 8 was applied to the inaugural total syntheses of fluostatin C and E.
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