Thermolyses of O-Phenyl Oxime Ethers. A New Source of Iminyl Radicals and a New Source of Aryloxyl Radicals

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1021/jo049927y
AuthorSearch for: 1; Search for: ; Search for: 1; Search for: ; Search for: ; Search for: 1
Affiliation
  1. National Research Council of Canada
FormatText, Article
SubjectDissociation; Enthalpy; Free radicals; Reaction kinetics; Synthesis (chemical); Cyclization; Hyperconjugation; Thermolyses; Ethers; ether derivative; imine; iminyl radical; n phenoxybenzimidic acid phenyl ether; o phenyl oxime ether derivative; oxyl radical; phenoxybenzamine; radical; unclassified drug; beta scission; binding competition; calculation; chemical analysis; chemical binding; chemical reaction kinetics; conjugation; cyclization; density functional theory; dissociation; enthalpy; product recovery; reaction analysis; room temperature; synthesis; temperature sensitivity; thermal analysis; thermolysis
Abstract
Publication date
In
LanguageEnglish
Peer reviewedYes
NPARC number21276655
Export citationExport as RIS
Report a correctionReport a correction (opens in a new tab)
Record identifier217b530b-6469-4c68-9bab-3af48ea6c0e2
Record created2015-10-13
Record modified2020-04-17
Date modified: