Transesterification of a Natural Epoxythymol Is Favored under Alkaline Conditions, Preserving the Enantiomeric Purity

Transesterification of a Natural Epoxythymol Is Favored under Alkaline Conditions, Preserving the Enantiomeric Purity

Transesterification is a synthetic chemistry strategy promoted in acid or alkaline conditions, yielding a structural diversity of organic compounds. Epoxythymols comprise a class of chiral natural compounds with biological relevance, and the literature describes their chiral purity loss during acid...

Full description

Saved in:
Bibliographic Details
Main Authors: Jessica M. Lorenzo-García, Antonio J. Oliveros-Ortiz, Héctor M. Arreaga-González, Carlos J. Cortés-García, Rosa E. del Río, Gabriela Rodríguez-García, Mario A. Gómez-Hurtado
Format: Article
Language:English
Published: MDPI AG 2023-11-01
Series:Chemistry Proceedings
Subjects:
epoxythymol
transesterification
chirality
Online Access:https://www.mdpi.com/2673-4583/14/1/30
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://www.mdpi.com/2673-4583/14/1/30

Similar Items