Organocatalytic strategies for the asymmetric functionalization of indoles

被引：509

作者：

Bartoli, Giuseppe ^{[1
]}

Bencivenni, Giorgio ^{[1
]}

Dalpozzo, Renato ^{[2
]}

机构：

[1] Univ Bologna, Dipartimento Chim Organ A Mangini, I-40136 Bologna, Italy

[2] Univ Calabria, Dipartimento Chim, I-87030 Arcavacata Di Rende, Cs, Italy

来源：

CHEMICAL SOCIETY REVIEWS | 2010年 / 39卷 / 11期

关键词：

FRIEDEL-CRAFTS ALKYLATION; CHIRAL PHOSPHORIC-ACID; PICTET-SPENGLER REACTIONS; ONE-POT SYNTHESIS; BRONSTED ACID; ALPHA; BETA-UNSATURATED KETONES; ENANTIOSELECTIVE SYNTHESIS; CATALYZED REACTIONS; CINCHONA ALKALOIDS; CARBONYL-COMPOUNDS;

D O I：

10.1039/b923063g

中图分类号：

O6 [化学];

学科分类号：

070301 [无机化学];

摘要：

The desire for new synthetic methodologies for the rapid construction of enantiomerically pure substituted indole has been a fruitful driving force for chemical research in the last few years. This research line has produced a stunning array of enantioselective technologies either metal or organocatalyzed. This critical review documents the development of organocatalytic indole alkylation strategies, until the end of 2009 (127 references).

引用

页码：4449 / 4465

页数：17

共 127 条

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