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Volumn 69, Issue 11, 2004, Pages 3937-3942

Effects of amine nature and nonleaving group substituents on rate and mechanism in aminolyses of 2,4-dinitrophenyl x-substituted benzoates

(5) Um, Ik Hwan a Kim, Kyung Hee a,c Park, Hye Ran a Fujio, Mizue b Tsuno, Yuho b

a Ewha Womans University (South Korea)

b KYUSHU UNIVERSITY (Japan)

c UNIVERSITY OF NOTRE DAME (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; CARBONYLATION; ELECTRONS; PHENOLS; RATE CONSTANTS; RESONANCE; SUBSTITUTION REACTIONS;

ELECTRON DONORS; ISOBASIC AMINES; NONLEAVING GROUPS;

AMINES;

2,4 DINITROPHENOL; AMINE; BENZOIC ACID DERIVATIVE; BENZYLAMINE; ETHANOLAMINE; ETHYLAMINE; ETHYLENEDIAMINE; GLYCINE; GLYCYLGLYCINE; MORPHOLINE; PIPERAZINE DERIVATIVE; PIPERIDINE DERIVATIVE; PROPYLAMINE; TRIFLUOROETHYLAMINE; UNCLASSIFIED DRUG;

AMINOLYSIS; ARTICLE; CHEMICAL REACTION; ENERGY; KINETICS; REACTION ANALYSIS; ULTRAVIOLET SPECTROSCOPY;

EID: 2442645211 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo049694a Document Type: Article

Times cited : (128)

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