4-hydroxycoumarin and related systems: Sitoselectivity of the Mitsunobu reaction with prenyl alcohols

被引：8

作者：

Cravotto, G

Nano, GM

Palmisano, G

Tagliapietra, S

机构：

[1] Univ Turin, Dipartimento Sci & Tecnol Farmaco, I-10125 Turin, Italy

[2] Univ Insubria, Dipartimento Sci Chim Fis & Matemat, I-22100 Como, Italy

来源：

HETEROCYCLES | 2003年 / 60卷 / 06期

关键词：

D O I：

10.3987/COM-03-9737

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Mitsunobu reaction leads to the formation of new C-C bonds between prenyl alcohols and 1,3-dicarbonyl compounds like 4-hydroxycoumarin or its nitrogen isoster. Buchapine was obtained through a one-pot procedure from 4-hydroxy-2-quinolone and dimethylallyl alcohol.

引用

页码：1351 / 1358

页数：8

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