| 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.
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											Authors
												Amy H. Yap, Steven M. Weinreb, 
											