An unprecedented concerted pathway in the alkaline hydrolysis of S-aryl thioesters

Journal of Organic Chemistry

Volumn 70, Issue 10, 2005, Pages 4203-4206

  Cevasco, Giorgio ^a   Thea, Sergio ^a  

^a CNR   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALKALINITY; HYDROLYSIS; PH EFFECTS; REACTION KINETICS;

ALKALINE SOLUTIONS; CLASSICAL MECHANISM; KINETIC DATA;

ESTERS;

2,4 DINITROPHENYL 4' HYDROXYTHIOBENZOATE; 2,4 DINITROPHENYL 4' METHOXYTHIOBENZOATE; 4 CYANOPHENYL 4' HYDROXYTHIOBENZOATE; 4 HYDROXYBENZOIC ACID ESTER; 4 NITROPHENYL 4' HYDROXYTHIOBENZOATE; ALKALI; AROMATIC HYDROCARBON; DIOXANE; KETENE DERIVATIVE; PENTACHLOROPHENYL 4' HYDROXYTHIOBENZOATE; PHENYL 4' HYDROXYTHIOBENZOATE; POTASSIUM CHLORIDE; THIOESTER; UNCLASSIFIED DRUG; WATER;

ARTICLE; CHEMICAL REACTION KINETICS; ENERGY; HYDROLYSIS; IONIC STRENGTH; IONIZATION; PH; PKA; REACTION ANALYSIS; SPECTROPHOTOMETRY; TEMPERATURE;

EID: 18744364918     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo050262p     Document Type: Article

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