| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5290440 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
A three-component coupling was used to prepare a series of 1,4-disubstituted-1,2,3-triazoles from the corresponding acetylated Baylis-Hillman adducts, sodium azide and terminal alkynes. This one-pot reaction further increases the efficacy of 'Click' synthesis and diversifies the preparation of multi-functional 1,4-disubstituted-1,2,3-triazoles.
Related Topics
Physical Sciences and Engineering
Chemistry
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Authors
S. Chandrasekhar, Debjit Basu, Ch. Rambabu,