A convenient synthesis of protoanemonin

被引：7

作者：

Crey, C ^{[1
]}

Dumy, P ^{[1
]}

Lhomme, J ^{[1
]}

Kotera, M ^{[1
]}

机构：

[1] Univ Grenoble 1, CNRS, UMR 5616, LEDSS, F-38041 Grenoble, France

来源：

SYNTHETIC COMMUNICATIONS | 2003年 / 33卷 / 21期

关键词：

protoanemonin; synthesis; beta- and delta-eliminations;

D O I：

10.1081/SCC-120025181

中图分类号：

O62 [有机化学];

学科分类号：

070303 [有机化学]; 081704 [应用化学];

摘要：

A new convenient synthesis of protoanemonin (1) starting from 2-deoxy-D-ribose (3) is described. A key step in the sequence is the successive beta- and delta-eliminations of 3,5-di-O-p-toluoyl-2-deoxy-D-ribono-1,4-lactone (6).

引用

页码：3727 / 3732

页数：6

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