A journey across recent advances in catalytic and stereoselective alkylation of indoles

被引:387
作者
Bandini, M
Melloni, A
Tommasi, S
Umani-Ronchi, A
机构
[1] Univ Bologna, Dipartimento Chim G Ciamician, I-40126 Bologna, Italy
[2] Politecn Milan, I-20133 Milan, Italy
关键词
alkylations; asymmetric catalysis; electrophilic aromatic substitutions; indoles; Lewis acids;
D O I
10.1055/s-2005-865210
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In this Account our recent results in relation to the catalytic and stereoselective Friedel-Crafts (FC) alkylation of indoles are described. Over the last decade, remarkable efforts have been devoted towards the replacement of the primal approaches with new more efficient, reliable, and environmentally benign strategies for the functionalization of indoles. Moreover, the emerging area of catalytic asymmetric FC processes is addressed and some examples of enantioselective alkylations of indoles via 1,4-addition to alpha,beta-unsaturated systems and asymmetric ring-opening reaction of aromatic epoxides are described.
引用
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页码:1199 / 1222
页数:24
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