Theoretical Study on the Epimerization of Azlactone Rings: Keto–Enol Tautomerism or Base-Mediated Racemization?
Author:
Affiliation:
1. Chemistry Department, Federal University of Juiz de Fora, Campus Martelos, Juiz de Fora, Minas Gerais 36036-900, Brazil
Funder
Funda??o de Amparo ? Pesquisa do Estado de Minas Gerais
Conselho Nacional de Desenvolvimento Cient?fico e Tecnol?gico
Coordena??o de Aperfei?oamento de Pessoal de N?vel Superior
Publisher
American Chemical Society (ACS)
Subject
General Chemical Engineering,General Chemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acsomega.8b00060
Reference44 articles.
1. Azlactone Reaction Developments
2. Oxazolones in Organocatalysis, New Tricks for an Old Reagent
3. The diverse chemistry of oxazol-5-(4H)-ones
4. Reactivity of Oxazol-5-(4H)-ones and Their Application toward Natural Product Synthesis
5. Peptide Synthesis via Active Esters. IV. Racemization and Ring-Opening Reactions of Opitcally Active Oxazolones
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