Journal
TETRAHEDRON LETTERS
Volume 42, Issue 42, Pages 7345-7348Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(01)01590-8
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A simple and efficient experimental protocol has been developed for the catalytic arylation of alkenes by the air and water stable. and phosphine-free compound PdCl2(SEt2)(2) associated vith tetrabutyl ammonium bromide. Using this catalytic protocol, aryl iodides and bromides. and electron-poor aryl chlorides Lire coupled with n-butylacrylate and styrene under relatively mild reaction conditions with high catalytic activity. Reaction vessel ultra-trace amounts (ppt) of this Pd precursor promotes the ccupling of iodo benzene with n-butylacrylate with turnover numbers (mol product mol Pd) Lip to 10 degrees. (C) 2001 Elsevier Science Lid. All rights reserved.
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