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: https://doi.org/10.1021/jo502710a
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  1. National Research Council of Canada
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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; chemical analysis; chemical reaction kinetics; chemical structure; reduction
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NPARC number21276502
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Record created2015-10-13
Record modified2020-04-22
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