Aminolysis of O-aryl thionobenzoates: Amine basicity combines with modulation of the nature of substituents in the leaving group and thionobenzoate moiety to control the reaction mechanism

Journal of Organic Chemistry

Volumn 73, Issue 19, 2008, Pages 7671-7677

  Um, Ik Hwan ^a   Hwang, So Jeong ^a   Yoon, Sora ^a,b   Jeon, Sang Eun ^a   Bae, Sun Kun ^a,c  

^a Ewha Womans University   (South Korea)

^b Environmental Research Complex   (South Korea)

^c Kunsan National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; AMINES; CHEMICAL REACTIONS; MODULATION; ORGANIC COMPOUNDS;

AMINOLYSIS; CHEMICAL EQUATIONS; KINETIC STUDIES; REACTION MECHANISMS;

AMINATION;

AMINE; BENZOIC ACID; CARBONYL DERIVATIVE; DIMETHYL SULFOXIDE; OXIDE;

AMINOLYSIS; ARTICLE; CHEMICAL ANALYSIS; CHEMICAL REACTION KINETICS; CHEMICAL STRUCTURE; PH; ULTRAVIOLET SPECTROPHOTOMETRY;

AMINES; BENZOATES; KINETICS;

EID: 53049083662     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo801539w     Document Type: Article

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