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
收藏
页码：4614 / 4618
页数：5
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