An Improved Synthesis of 2-Aryl-1,1-bis(trimethylsilyl)ethenes

被引:1
作者
Pawluc, Piotr [1 ]
Hreczycho, Grzegorz [1 ]
Madalska, Martyna [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
SYNTHESIS-STUTTGART | 2009年 / 22期
关键词
bis(silyl)alkene; Heck reaction; Grignard reaction; cross coupling; organometallic reagent; PALLADIUM-CATALYZED ARYLATION; FACILE SYNTHESIS; SILVER-NITRATE; STEREOSELECTIVE APPROACH; REAGENTS; 1,1-DISILYLETHENES; HYDROSILYLATION; VINYLSILANES; OLEFINATION; ACYLSILANES;
D O I
10.1055/s-0029-1218155
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A series of new 2-aryl-1,1-bis(trimethylsilyl)ethenes containing ortho-, meta-, and para-substituted aryl or heteroaryl groups has been efficiently synthesized using an improved two-step approach based on a silylative Coupling cyclization-Heck coupling/Grignard reaction sequence. The crystal structure of the first 1,1-bis(trimethylsilyl)alk-1-ene containing a heteroaryl group is reported.
引用
收藏
页码:3843 / 3847
页数:5
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