Complementary stereoselective conjugate addition reactions on indolo[2,3-α]-quinolizine templates

被引:19
作者
Allin, SM [1 ]
Khera, JS
Thomas, CI
Witherington, J
Doyle, K
Elsegood, MRJ
Edgar, M
机构
[1] Univ Loughborough, Dept Chem, Loughborough LE11 3TU, Leics, England
[2] GlaxoSmithKline Res Ltd, Dept Med Chem, Neurol & GI Ctr Excellence Drug Discovery, Harlow CM19 5AW, Essex, England
[3] OSI Pharmaceut, Oxford OX4 6LT, England
关键词
D O I
10.1016/j.tetlet.2006.01.081
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We report a new and highly stereoselective approach for the construction of a range of functionalized indolo[2,3-a]quinolizine targets from a readily available, nonracemic chiral template. The methods developed allow us to predetermine relative product stereochemistries by judicious choice of substrate sub-structure. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1961 / 1964
页数:4
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