5-Endo-trig radical cyclizations

被引：112
|
作者：
Ishibashi, H [1 ]
Sato, T
Ikeda, M
机构：
[1] Kanazawa Univ, Fac Pharmaceut Sci, Kanazawa, Ishikawa 9200934, Japan
[2] Kyoto Pharmaceut Univ, Yamashina, Kyoto 6078414, Japan
来源：
SYNTHESIS-STUTTGART | 2002年 / 06期
关键词：
alkaloids; tributyltin hydride; cyclizations; 5-endo-trig; alpha-halo amides; manganese(III) acetate; radicals;
D O I：
10.1055/s-2002-25759
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
5-Endo-trig ring-closure is recognized as a disfavored process. However, a number of examples of such a type of cyclization have recently been reported. This review focuses on studies of 5-endo-trig radical cyclizations that provide new syntheses of five-membered carbo- and heterocyclic compounds.
引用
收藏
页码：695 / 713
页数：19
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