New One-Pot Synthesis of (E)-β-Aryl Vinyl Halides from Styrenes

被引：51
|
作者：
Pawluc, Piotr [1 ]
Hreczycho, Grzegorz [1 ]
Szudkowska, Justyna [1 ]
Kubicki, Maciej [1 ]
Marciniec, Bogdan [1 ]
机构：
[1] Adam Mickiewicz Univ Poznan, Fac Chem, Dept Organometall Chem, PL-60780 Poznan, Poland
来源：
ORGANIC LETTERS | 2009年 / 11卷 / 15期
关键词：
HIGHLY STEREOSELECTIVE-SYNTHESIS; ALPHA; BETA-UNSATURATED CARBOXYLIC-ACIDS; CATALYTIC HUNSDIECKER REACTION; OLEFIN CROSS-METATHESIS; ORGANIC-SYNTHESIS; TERMINAL ALKYNES; BROMIDES; VINYLSILANES; CONVERSION; REDUCTION;
D O I：
10.1021/ol901233j
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
A new, efficient protocol for the highly stereoselective one-pot synthesis of (E)-beta-aryl vinyl iodides and (E)-beta-aryl vinyl bromides from styrenes based on sequential ruthenium-catalyzed silylative coupling-N-halosuccinimide-mediated halodesilylation reactions is reported.
引用
收藏
页码：3390 / 3393
页数：4
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