A highly stereoselective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis

被引:28
作者
Allin, SM [1 ]
Thomas, CI
Allard, JE
Doyle, K
Elsegood, MRJ
机构
[1] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[2] OSI Pharmaceut, Oxford OX4 6LT, England
关键词
natural products; heterocycles; lactams; asymmetric synthesis;
D O I
10.1002/ejoc.200500412
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We present a facile and highly stereoselective approach to the indolo[2,3-alpha]quinolizine ring system from a readily available, non-racemic chiral template. We demonstrate the potential for application of this methodology to natural product synthesis through conversion of the template to some representative indole alkaloids with high enantiomeric purity in both enantiomeric series.
引用
收藏
页码:4179 / 4186
页数:8
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