通过金催化的级联环化反应立体选择性合成四环吲哚啉。
Stereoselective synthesis of tetracyclic indolines via gold-catalyzed cascade cyclization reactions.
机构信息
Dipartimento di Chimica G. Ciamician, Alma Mater Studiorum-Università di Bologna, via Selmi 2, Bologna I-40126, Italy.
出版信息
Chem Commun (Camb). 2011 Jul 21;47(27):7803-5. doi: 10.1039/c1cc12328a. Epub 2011 Jun 1.
PMID:21633749
Abstract
A reliable synthetic route to fused polycyclic indolines is documented by the development of a stereoselective gold catalyzed cascade cyclization of indole propargylic alcohols.
摘要
本文报道了一种通过吲哚炔丙醇的立体选择性金催化级联环化反应来合成稠合多环吲哚啉的可靠方法。
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