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Copper-catalyzed click synthesis of functionalized 1,2,3-triazoles with 3,4-dihydropyrimidinone or amide group via a one-pot four-component reaction

Authors :
Quan, Zheng-Jun
Xu, Qiong
Zhang, Zhang
Da, Yu-Xia
Wang, Xi-Cun
Source :
Tetrahedron. Jan2013, Vol. 69 Issue 2, p881-887. 7p.
Publication Year :
2013

Abstract

Abstract: A Cu (I) generated in situ from Cu(OAc)2·H2O/sodium ascorbate catalyzed one-pot multicomponent reaction for the synthesis of a series of N-functionalized 1,2,3-triazoles with 3,4-dihydropyrimidione from 3,4-dihydropyrimidiones, paraformaldehyde, sodium azide and alkynes is described. Remarkably N-functionalized 1,2,3-triazoles with amide were prepared by this method. This procedure eliminates the need to handle organic halides or organic azides, as they are generated in situ, making this already powerful click process even more user-friendly and safe. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404020
Volume :
69
Issue :
2
Database :
Academic Search Index
Journal :
Tetrahedron
Publication Type :
Academic Journal
Accession number :
84555451
Full Text :
https://doi.org/10.1016/j.tet.2012.10.097