Preparation of (E)-1-aryl-3,3,3-trifluoro-1,2-di(trimethylsilyl)-1-propenes via stereoselective bissilylation of trifluoromethyl aryl acetylenes and electrophilic substitution of its TMS groups

被引:5
|
作者
Katagiri, Toshimasa [1 ]
Nakanishi, Hayato [1 ]
Ohno, Kenichi [1 ]
Seiki, Takayuki [1 ]
Isobe, Akira [1 ]
Kataoka, Keisuke [1 ]
Uneyama, Kenji [1 ]
机构
[1] Okayama Univ, Fac Engn, Dept Appl Chem, Kita Ku, Okayama 7008530, Japan
关键词
Reductive bissilylation; Trifluoromethylated olefin; Trifluoropropene; Stereoselective anti addition; INTRAMOLECULAR BIS-SILYLATION; PALLADIUM-CATALYZED REACTIONS; TERT-ALKYL ISOCYANIDE; BONDS; ACTIVATION; STEREOCHEMISTRY;
D O I
10.1016/j.tet.2011.03.005
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Preparations and reactions of (E)-1-aryl-3,3,3-trifluoro-1,2-di(trimethylsilyl)-1-propenes are described. (E)-1-Aryl-3,3,3-trifluoro-1,2-di(trimethylsilyl)-1-propene was prepared from aryl trifluoromethyl acetylenes via reductive bissilylation by TMSCl/Mg in good yields. The silyl groups of (E)-3,3,3-trifluoro-1,2-di (trimethylsilyl)-1-phenyl-1-propene were substituted by electrophiles in both a stepwise and stereoselective (and/or stereospecific) manner. This compound could be a building block for preparations of substituted trifluoropropenes. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3041 / 3045
页数:5
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