第一作者:Hongbin Sun
通讯作者:Ruimao Hua
合写作者:Songjie Chen, Yingwu Yin
发表刊物:Advanced Synthesis & Catalysis
期号:14
卷号:348
影响因子:4.4
DOI码:10.1002/adsc.200606157
所属单位:Department of Chemistry, Tsinghua University
教研室:物理化学
刊物所在地:GERMANY
摘要:In the presence of catalytic amount of bismuth(III) chloride, the reactions of acyl chlorides or vinyl chlorides with arenes afforded 1,1-diarylalkenes in 25–82 % isolated yield. In the case of the reaction of acyl chlorides with arenes, the procedure includes an initial Friedel–Crafts acylation, subsequent formation of vinyl chlorides and final Friedel–Crafts-type vinylation of another arene molecule with vinyl chloride. This paper reports the first Lewis acid-catalyzed cleavage of the CCl bond of vinyl chloride and its application in the synthesis of multiply subtituted alkenes.
关键字:acyl chlorides; arenes; bismuth(III) chlo-ride; 1,1-diarylalkenes; Friedel–Crafts reaction; vinylchlorides
论文编号:WOS:000240707900019
学科门类:理学
一级学科:化学
页面范围:1919-1925
ISSN号:1615-4150
是否译文:否
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