128979-27-1Relevant articles and documents
Hetero-Diels-Alder reactions of novel 3-triazolyl-nitrosoalkenes as an approach to functionalized 1,2,3-triazoles with antibacterial profile
Lopes, Susana M.M.,Novais, Juliana S.,Costa, Dora C.S.,Castro, Helena C.,Figueiredo, Agnes Marie S.,Ferreira, Vitor F.,Pinho e Melo, Teresa M.V.D.,da Silva, Fernando de Carvalho
, p. 1010 - 1020 (2017/12/15)
The generation and reactivity of 3-triazolyl-nitrosoalkenes are reported for the first time. The study showed that hetero-Diels-Alder reaction of these heterodienes is an interesting synthetic strategy to functionalized 1,2,3-triazoles, including 1,2,3-tr
Copper(I)-catalyzed aerobic oxidative azide-alkene cyclo-addition: An efficient synthesis of substituted 1,2,3-triazoles
Janreddy, Donala,Kavala, Veerababurao,Kuo, Chun-Wei,Chen, Wen-Chang,Ramesh, Chintakunta,Kotipalli, Trimurtulu,Kuo, Ting-Shen,Chen, Mei-Ling,He, Chiu-Hui,Yao, Ching-Fa
, p. 2918 - 2927 (2014/03/21)
A novel, copper(I)-promoted azide-alkene aerobic oxidative cycloaddition protocol was devel-oped for the regioselective synthesis of 1,4-disubsti-tuted/ 1,4,5-trisubstituted 1,2,3-triazoles by using azides and electron-deficient olefins under an oxygen atmosphere.