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

Journal of Organic Chemistry

Volumn 80, Issue 3, 2015, Pages 1321-1331

  Ingold, K U ^a,b   Bowry, Vincent W ^b  

^a NATIONAL RESEARCH COUNCIL CANADA   (Canada)

^b JAMES COOK UNIVERSITY   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

INTEGRAL 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;

EID: 84922723590     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo502710a     Document Type: Article

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