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Nickel-catalyzed, sodium iodide-promoted reductive dimerization of alkyl halides, alkyl pseudohalides, and allylic acetates†
Michael R. Prinsell,Daniel A. Everson,Daniel J. Weix
Chemical Communications Pub Date : 06/28/2010 00:00:00 , DOI:10.1039/C0CC01716G
Abstract

The first general method for the reductive dimerization of alkyl halides, alkyl mesylates, alkyl trifluoroacetates, and allylic acetates is reported which proceeds with low catalyst loading (0.5 to 5 mol%), generally high yields (80% ave yield), and good functional-group tolerance.

Graphical abstract: Nickel-catalyzed, sodium iodide-promoted reductive dimerization of alkyl halides, alkyl pseudohalides, and allylic acetates
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