Cycloaddition of homochiral imidazolinium ylides: A route to optically active pyrroloimidazoles

被引：48
作者：
Jones, RCF
Howard, KJ
Snaith, JS
机构：
[1] Department of Chemistry, University of Nottingham, Nottingham NG7 2RD, University Park
[2] Chemistry Department, Open University, Walton Hall
来源：
TETRAHEDRON LETTERS | 1996年 / 37卷 / 10期
关键词：
D O I：
10.1016/0040-4039(96)00113-X
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
The synthesis of either enantiomer of 1-benzyl-4-phenyl-2-imidazoline from phenylglycine is described. 'One-pot' generation and enantioselective 1,3-dipolar cycloaddition of homochiral azomethine ylides prepared from these imidazolines with a range of alkene dipolarophiles affords optically active hexahydropyrroloimidazole adducts.
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页码：1707 / 1710
页数：4
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