Intermolecular Mizoroki–Heck Reaction of Aliphatic Olefins with High Selectivity for Substitution at the Internal Position
L Qin, X Ren, Y Lu, Y Li, JS Zhou
Index: Qin, Liena; Ren, Xinfeng; Lu, Yunpeng; Li, Yongxin; Zhou, Jianrong Angewandte Chemie - International Edition, 2012 , vol. 51, # 24 p. 5915 - 5919
Full Text: HTML
Citation Number: 46
Abstract
The Mizoroki–Heck reaction generally refers to Pd-catalyzed CÀC bond formation between organic (pseudo) halides and olefins. Today, it has become a powerful tool to prepare substituted olefins.[1] A key issue in intermolecular Heck reactions is the control of the site where aryl groups insert into olefins. High regioselectivity can be easily achieved for olefins carrying substituents with a significant electronic difference at the two olefinic sites,[2] such ...
Related Articles:
Über Perfluoralkansulfonsäurearylester
[Niederpruem,H. et al. Justus Liebigs Annalen der Chemie, 1973 , p. 20 - 32]
Über Perfluoralkansulfonsäurearylester
[Niederpruem,H. et al. Justus Liebigs Annalen der Chemie, 1973 , p. 20 - 32]