Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5290434 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
β-Tosylethylazide (TSE-N3), which can be prepared in one step from p-tolyl vinyl sulfone and sodium azide/H2SO4, undergoes metal-catalyzed 1,3-dipolar cycloadditions with alkynes to produce TSE-protected 1,2,3-triazoles. The protecting group can be removed using potassium tert-butoxide in THF at â78 to 0 °C.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Amy H. Yap, Steven M. Weinreb,