Silver-catalyzed direct selenylation of terminal alkynes through C-H bond functionalization

被引:23
|
作者
Xavier, Mauricio C. D. F. [1 ]
Goldani, Bruna [1 ]
Schumacher, Ricardo F. [1 ]
Perin, Gelson [1 ]
Schneider, Paulo Henrique [2 ]
Alves, Diego [1 ]
机构
[1] Univ Fed Pelotas, UFPel, CCQFA, Lab Sintese Organ Limpa,LASOL, POB 354, BR-35496010 Pelotas, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Inst Quim, UFRGS, Porto Alegre, RS, Brazil
来源
MOLECULAR CATALYSIS | 2017年 / 427卷
关键词
C-H Functionalization; Alkynes; Silver; Selenium; Catalysis; HIGHLY EFFICIENT; CHALCOGENIDES SELENIDES; CYCLOADDITION REACTIONS; SYNTHETIC ROUTE; ACTIVATION; TELLURIDES; DICHALCOGENIDES; CYCLIZATION; ACETYLENES; WATER;
D O I
10.1016/j.molcata.2016.11.033
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We described herein the use of a silver catalyst in the selenylation of terminal alkynes by direct C-H functionalization. These reactions were performed under mild conditions, reacting a range of terminal alkynes with different diorganyl diselenides using AgNO3 (10 mol-%) as catalyst in CH2Cl2 at 25 degrees C under air atmosphere. This is an efficient and general cross-coupling reaction and was performed with alkynes and diorganyl diselenides bearing electron-withdrawing and electron-donating groups affording the corresponding selanylalkynes in good to excellent yields. (C) 2016 Published by Elsevier B.V.
引用
收藏
页码:73 / 79
页数:7
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