部分
化学
三萜类
多米诺骨牌
立体化学
对映选择合成
立体选择性
三萜
组合化学
立体异构
分子
有机化学
催化作用
医学
病理
替代医学
作者
Andrei Corbu,Maurizio Aquino,T. V. Pratap,Pascal Retailleau,Siméon Arseniyadis
出处
期刊:Organic Letters
[American Chemical Society]
日期:2008-04-09
卷期号:10 (9): 1787-1790
被引量:21
摘要
The monocyclic triterpene iridal 1 (parent molecule) is synthesized by an approach that allows access for several representatives of the iridal family as well as diversely substituted analogues. The success of the proposed synthetic plan depends upon the effortless stereoselective establishment of the trans C10/C11 dimethyl relationship in B-ring moiety 7 using a domino-based methodology and the higly efficient Miyaura-Suzuki type sp3-sp2 segment coupling 7 and 8, respectively.
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