| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5269066 | Tetrahedron Letters | 2014 | 4 Pages |
Abstract
- N-Unsubstituted isoxazolines result from 1,3-cycloadditions of oxime and alkenes.
- N-Functionalizations of isoxazolidines with chemically active groups are described.
- A new approach to nucleoside analogues from isoxazolidines is presented.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Carlos A.D. Sousa, José E. RodrÃguez-Borges, Xerardo Garcia-Mera,