通过钯催化的α-芳基化反应实现少花 F 和相关茚满酮类似物的简洁合成。
A concise synthesis of paucifloral F and related indanone analogues via palladium-catalyzed α-arylation.
机构信息
Genomics Institute of the Novartis Research Foundation, 10675 John Jay Hopkins Drive, San Diego, California 92121, USA.
出版信息
J Org Chem. 2011 Mar 18;76(6):1902-5. doi: 10.1021/jo102298p. Epub 2011 Feb 3.
PMID:21291249
Abstract
A concise approach to synthesize paucifloral F was developed via a stereoselective palladium-catalyzed α-arylation reaction. The approach has also been applied in the synthesis of indanone analogues of Paucifloral F.
摘要
发展了一种简洁的方法，通过立体选择性钯催化的α-芳基化反应来合成少瓣 F。该方法也已应用于少瓣 F 的茚满酮类似物的合成。
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