Strategies for the asymmetric functionalization of indoles: an update

被引：349

作者：

Dalpozzo, Renato ^{[1
]}

机构：

[1] Univ Calabria, Dipartimento Chim & Tecnol Chim, Cubo 12-C, I-87036 Arcavacata Di Rende, Cs, Italy

来源：

CHEMICAL SOCIETY REVIEWS | 2015年 / 44卷 / 03期

关键词：

FRIEDEL-CRAFTS ALKYLATION; DIELS-ALDER REACTION; GENERATED IN-SITU; PICTET-SPENGLER REACTIONS; N-TRIFLYL PHOSPHORAMIDE; ENANTIOSELECTIVE SYNTHESIS; MICHAEL ADDITION; ALPHA; BETA-UNSATURATED ALDEHYDES; ORGANOCATALYTIC CONSTRUCTION; FLUORENE DERIVATIVES;

D O I：

10.1039/c4cs00209a

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

During the past four years, the research of new synthetic methodologies for the rapid construction of enantiomerically pure substituted indole has had a fruitful and important growth. This research line continues to produce stunning arrays of enantioselective technologies either metal or organocatalyzed. Thus, an update of our previous review (Chem. Soc. Rev., 2010, 39, 4449-4465) has become necessary and this critical review documents the literature on this topic, until the end of 2013.

引用

页码：742 / 778

页数：37

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