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Journal of the American Chemical Society

Volumn 135, Issue 19, 2013, Pages 7349-7354

Dissociation or cyclization: Options for a triad of radicals released from oxime carbamates

(2) McBurney, Roy T a,b Walton, John C a

a UNIVERSITY OF ST ANDREWS (United Kingdom)

b UNIVERSITY OF GLASGOW (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

5-EXO CYCLIZATION; CARBONYLDIIMIDAZOLE; EPR SPECTROSCOPY; IMINYL RADICALS; PHENANTHRIDINE; RATE PARAMETERS; ROOM TEMPERATURE; UV PHOTOLYSIS;

KETONES; ORGANIC COMPOUNDS; PARAMAGNETIC RESONANCE; PHOTOLYSIS; RATE CONSTANTS;

CYCLIZATION;

ACETOPHENONE; CARBAMIC ACID; DIETHYLAMINE; NITROGEN; OXIME; OXYGEN; PHENANTHRIDINE DERIVATIVE; RADICAL; VOLATILE AGENT;

ARTICLE; CHEMICAL BOND; CHEMICAL PARAMETERS; CYCLIZATION; DENSITY FUNCTIONAL THEORY; DISSOCIATION; ELECTRON SPIN RESONANCE; ENERGY; ENTHALPY; PHOTOLYSIS; PROTON NUCLEAR MAGNETIC RESONANCE; RADICAL REACTION; ROOM TEMPERATURE;

CARBAMATES; CYCLIZATION; ELECTRON SPIN RESONANCE SPECTROSCOPY; MODELS, MOLECULAR; OXIMES; PHOTOLYSIS; ULTRAVIOLET RAYS;

EID: 84877793902 PISSN: 00027863 EISSN: 15205126 Source Type: Journal
DOI: 10.1021/ja402833w Document Type: Article

Times cited : (64)

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