Highly efficient formation of nitriles and alkoxy radicals from N-alkoxybenziminoyl chlorides in solution

Journal of Organic Chemistry

Volumn 74, Issue 4, 2009, Pages 1679-1684

  De Peter Lijser, H J ^a   Burke, Cassandra R ^a   Rosenberg, Jonathan ^a   Hunter, Jordan ^a  

^a CALIFORNIA STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKOXY RADICALS; HIGH CONCENTRATIONS; HYDROGEN ATOMS; HYDROGEN-ATOM TRANSFERS; LOWER LIMITS; SCISSION PROCESS; SCISSION REACTIONS; TRIBUTYLTIN HYDRIDES;

ATOMS; CHLORINE COMPOUNDS; CYANIDES; HYDROGEN; ORGANIC SOLVENTS; RATE CONSTANTS; TOLUENE;

FREE RADICAL REACTIONS;

ALKOXY RADICAL; BENZALDEHYDE DERIVATIVE; CARBON; CHLORIDE; ETHER; HYDROGEN; N ALKOXYBENZIMINOYL CHLORIDE; NITRILE; OXIME; OXYGEN; RADICAL; SOLVENT; STEROID; TOLUENE; TRIBUTYLTIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; GAS CHROMATOGRAPHY; REACTION ANALYSIS; SYNTHESIS;

EID: 64349117858     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo8026142     Document Type: Article

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