| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5226142 | Tetrahedron | 2006 | 7 Pages |
Abstract
Primary, secondary, and aromatic azides undergo 1,3 dipolar cycloaddition-coupling with an excess of alkyne in the presence of Cu(CH3CN)4PF6 as catalyst, N,N,Nâ²-trimethylethylenediamine as ligand, molecular oxygen, and 4-methoxymorpholine N-oxide (NMO) as co-oxidant to afford 1,4,5-trisubstituted-1,2,3-triazoles.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Baudouin Gerard, Jamie Ryan, Aaron B. Beeler, John A. Jr.,