Efficient synthesis of selenol esters from acid chlorides mediated by indium metal

被引：47

作者：

Marin, Graciane ^{[1
]}

Braga, Antonio L. ^{[1
,2
]}

Rosa, Anderson S. ^{[1
]}

Galetto, Fabio Z. ^{[1
]}

Burrow, Robert A. ^{[1
]}

Gallardo, Hugo ^{[2
]}

Paixao, Marcio W. ^{[1
,3
]}

机构：

[1] Univ Fed Santa Maria, Dept Quim, BR-97105900 Santa Maria, RS, Brazil

[2] Univ Fed Santa Catarina, Dept Quim, BR-88040900 Florianopolis, SC, Brazil

[3] Univ Sao Paulo, Inst Quim, BR-05508900 Sao Paulo, Brazil

来源：

TETRAHEDRON | 2009年 / 65卷 / 23期

基金：

巴西圣保罗研究基金会;

关键词：

RING-OPENING REACTION; TELLUROL ESTERS; STRAIGHTFORWARD SYNTHESIS; DIPHENYL DISELENIDE; DIORGANYL SELENIDES; CRYSTAL-STRUCTURES; PROMOTED CLEAVAGE; ACYL RADICALS; ALKYL; ORGANOSELENIUM;

D O I：

10.1016/j.tet.2009.03.069

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

This article describes an efficient and easy one-pot route for the synthesis of a wide range of selenol esters from acyl chloride with diselenides in the presence of indium metal. A variety of functional groups can be tolerated within the diorgano diselenide and the acyl chloride coupling partner. (C) 2009 Elsevier Ltd. All rights reserved.

引用

页码：4614 / 4618

页数：5

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