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Rhodium(II)‐Catalyzed Nondirected Oxidative Alkenylation of Arenes: Arene Loading at One Equivalent
Author(s) -
Vora Harit U.,
Silvestri Anthony P.,
Engelin Casper J.,
Yu JinQuan
Publication year - 2014
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201310539
Subject(s) - rhodium , bimetallic strip , catalysis , phosphine , chemistry , ligand (biochemistry) , oxidative addition , umpolung , medicinal chemistry , combinatorial chemistry , organic chemistry , receptor , biochemistry , nucleophile
A bimetallic Rh II catalyst promoted the CH alkenylation of simple arenes at 1.0 equivalent without the use of a directing group. A phosphine ligand as well as cooperative reoxidation of Rh II with Cu(TFA) 2 and V 2 O 5 proved essential in providing monoalkenylated products in good yields and selectivities, especially with di‐ and trisubstituted arenes.

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