The mechanism of the hydrolysis of acylimidazoles in aqueous mineral acids. The excess acidity method for reactions that are not acid catalyzed

Canadian Journal of Chemistry

Volumn 75, Issue 8, 1997, Pages 1093-1098

  Cox, Robin A ^a  

^a UNIVERSITY OF TORONTO   (Canada)

Author keywords

Acylimidazoles; Excess acidity; Hydrolysis; Protonation; Tetrahedral intermediate

Indexed keywords

AROMATIC COMPOUNDS; CATALYSIS; HYDROCHLORIC ACID; HYDROLYSIS; PH EFFECTS; REACTION KINETICS; SOLUTIONS; SUBSTRATES; SULFURIC ACID; THERMAL EFFECTS;

EXCESS ACIDITY METHOD; IMIDAZOLES; PERCHLORIC ACID; PROTONATION;

NITROGEN COMPOUNDS;

HYDROCHLORIC ACID; HYDROXIDE; IMIDAZOLE DERIVATIVE; INORGANIC ACID; N ACETYLIMIDAZOLE; PERCHLORIC ACID; SULFURIC ACID;

ANALYTIC METHOD; AQUEOUS SOLUTION; ARTICLE; CHEMICAL REACTION KINETICS; DECOMPOSITION; HYDROLYSIS; INTERMETHOD COMPARISON; PH; PROTON TRANSPORT;

EID: 0031213957     PISSN: 00084042     EISSN: None     Source Type: Journal    
DOI: 10.1139/v97-129     Document Type: Article

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