Efficient [3,3]-sigmatropic rearrangement accelerated by a trifluoroacetyl group: synthesis of benzofurans under mild conditions

被引：26

作者：

Miyata, O ^{[1
]}

Takeda, N ^{[1
]}

Morikami, Y ^{[1
]}

Naito, T ^{[1
]}

机构：

[1] Kobe Pharmaceut Univ, Kobe, Hyogo 6588558, Japan

来源：

ORGANIC & BIOMOLECULAR CHEMISTRY | 2003年 / 1卷 / 02期

关键词：

D O I：

10.1039/b210059b

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The [3,3]-sigmatropic rearrangement took place smoothly during the course of trifluoroacetylation of O-phenyloxime at below room temperature to give the dihydrobenzofuran or benzofuran as a result of concomitant cyclization.

引用

页码：254 / 256

页数：3

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