Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5285271 | Tetrahedron Letters | 2008 | 5 Pages |
Abstract
Isoxazole-linked steroidal glycoconjugates are prepared by 1,3-dipolar cycloaddition reactions of an in situ generated and hitherto unknown steroidal nitrile oxide with appropriate propargyl ethers of sugars. The methodology provides a novel vector in the form of an easily accessible nitrile oxide having the ability to couple with a host of biomolecules, thus offering a new pathway to construct biologically significant steroidal conjugates.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Karuna S. Wankhede, Vipraja V. Vaidya, Prajakta S. Sarang, Manikrao M. Salunkhe, Girish K. Trivedi,