Why are organotin hydride reductions of organic halides so frequently retarded? kinetic studies, analyses, and a few remedies

From National Research Council Canada

DOIResolve DOI: http://doi.org/10.1021/jo502710a
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  1. National Research Council Canada
Journal titleJournal of Organic Chemistry
Pages13211331; # of pages: 11
SubjectIntegral equations; Kinetic theory; Kinetics; Organic solvents; Organometallics; Rate constants; Repair; Tin; Chain transfer rates; Hydride reduction; Model kinetic equations; Organic halides; Propagation step; Radical chain; Reaction conditions; Side reactions; Chains; anthracene; benzophenone; cyclohexane; organohalogen derivative; organotin compound; radical; addition reaction; Article; chemical analysis; chemical reaction kinetics; chemical structure; reduction
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Peer reviewedYes
NPARC number21276502
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Record identifierdcb1e8a5-b43b-4338-9c28-be364784f2c7
Record created2015-10-13
Record modified2016-05-09
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