ZrO2-supported Cu(II)-β-cyclodextrin complex: construction of 2,4,5-trisubstituted-1,2,3-triazoles via azide-chalcone oxidative cycloaddition and post-triazole alkylation

被引:36
|
作者
Girish, Yarabally R. [1 ]
Kumar, Kothanahally S. Sharath [1 ]
Muddegowda, Umashankar [2 ]
Lokanath, Neartur Krishnappagowda [3 ]
Rangappa, Kanchugarakoppal S. [1 ]
Shashikanth, Sheena [1 ]
机构
[1] Univ Mysore, Dept Studies Chem, Mysore 570006, Karnataka, India
[2] KSOU, Dept Studies Chem, Mysore 570006, Karnataka, India
[3] Univ Mysore, Dept Studies Phys, Mysore 570006, Karnataka, India
关键词
ONE-POT SYNTHESIS; CLICK-CHEMISTRY; REGIOSELECTIVE SYNTHESIS; TERMINAL ALKYNES; SODIUM-AZIDE; EFFICIENT SYNTHESIS; HIV-1; PROTEASE; BORONIC ACIDS; 1,2,3-TRIAZOLES; NANOPARTICLES;
D O I
10.1039/c4ra09970b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
An efficient one-pot three-component stepwise approach for the synthesis of N-2-substituted-1,2,3-triazoles from chalcones, sodium azide and esters has been developed using a recoverable and reusable ZrO2 nanoparticle-supported Cu(II)-beta-cyclodextrin complex as a catalyst. N-2 alkylation of triazoles using different aryl-alkyl esters without any additives has been achieved for the first time. The one-pot operation, atom-economical nature, regioselectivity and good yields are the noteworthy features of this protocol. The reusability of the prepared nanocatalyst was successfully examined four times without any appreciable loss in catalytic activity.
引用
收藏
页码:55800 / 55806
页数:7
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