| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5261823 | Tetrahedron Letters | 2015 | 7 Pages |
Abstract
A novel strategy towards the construction of highly diversified tetrahydroquinolinoisoxazole frameworks with high diastereoselectivity via intramolecular 1,3-dipolar nitrone cycloaddition reaction is described for the first time. All the synthesized tetrahydroquinolinoisoxazoles are new and obtained in excellent yields under catalyst free condition.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Manickam Bakthadoss, Anthonisamy Devaraj,