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Steric effects in the nucleophilic versus general base-catalysed intramolecular carboxy-group-assisted solvolysis of esters
Journal of the Chemical Society D: Chemical Communications Pub Date : , DOI:10.1039/C29700001389
Abstract

Intramolecular participation by carboxylate anion in the solvolysis of the hindered ester 2-carboxyphenyl mesitoate in anhydrous methanol, occurs entirely by a nucleophilic mechanism in contrast to aspirin which previously has been shown to involve the kinetically equivalent general base mechanism.

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