SN2 Mechanism for Alcoholysis, Aminolysis, and Hydrolysis of Acetyl Chloride
Author:
Affiliation:
1. Department of Chemistry, University of Wales Swansea, Singleton Park, Swansea SA2 8PP, Wales, UK
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9609844
Reference88 articles.
1. Is SN2 Substitution with Inversion of Configuration at Vinylic Carbon Feasible?
2. SN2 and AdN-E Mechanisms in Bimolecular Nucleophilic Substitutions at Vinyl Carbon. The Relevance of the LUMO Symmetry of the Electrophile
3. Stepwise versus Concerted Mechanisms at Trigonal Carbon: Transfer of the 1,3,5-Triazinyl Group between Aryl Oxide Ions in Aqueous Solution
4. Concertedness in acyl group transfer in solution: a single transition state in acetyl group transfer between phenolate ion nucleophiles
5. Structure-reactivity correlations for reactions of substituted phenolate anions with acetate and formate esters
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