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

被引:35
作者
Allin, SM [1 ]
Thomas, CI
Allard, JE
Doyle, K
Elsegood, MRJ
机构
[1] Loughborough Univ Technol, Dept Chem, Loughborough LE11 3TU, Leics, England
[2] OSI Pharmaceut, Oxford OX4 6LT, England
关键词
D O I
10.1016/j.tetlet.2004.07.121
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report a novel, facile and highly stereoselective approach to the indolo[2,3-a]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 a simple indole alkaloid with high enantiomeric purity. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7103 / 7105
页数:3
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