Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5419243 | Journal of Molecular Structure: THEOCHEM | 2007 | 4 Pages |
Abstract
The ring contraction of trans-5-hydroxy-1,3-oxazin-2-ones 1 into cis-5-hydroxymethyl-oxazolidinones 3 was studied with different bases and nucleophiles and it was found that it is the basicity and not the nucleophilicity the factor responsible for the ring contractions. A DFT study was made for the proposed mechanism.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
A. Hamdach, R.J. Zaragozá, E. Zaballos-GarcÃa, J. Sepúlveda-Arques,