1034194-35-8Relevant articles and documents
Efficient copper-catalyzed tandem oxidative iodination and alkyne-azide cycloaddition in the presence of glycine-type ligands
Yuan, Donghe,Wang, Shilei,Zhu, Gongming,Zhu, Anlian,Li, Lingjun
, (2021)
Tandem oxidative iodination and alkyne-azide cycloaddition reaction has provided one of the most widely used methods for preparation of 5-iodo-1,2,3-triazoles. However, stoichiometric copper salts are involved in this type of reaction in order to enhance
Supported NHC-Benzimi@Cu Complex as a Magnetically Separable and Reusable Catalyst for the Multicomponent and Click Synthesis of 1,4-Disubstituted 1,2,3-Triazoles via Huisgen 1,3-Dipolar Cycloaddition
Chandane, Wilson,Gajare, Shivanand,Jagdale, Ashutosh,Patil, Sandip,Patil, Suresh,Pawar, Arvind,Rashinkar, Gajanan
, (2021/08/23)
In this paper, we report a novel magnetically separable silica coated copper nano-magnetite NHC-benzimi@Cu complex as heterogeneous catalyst for the multicomponent click reaction via Huisgen 1,3-dipolar cycloaddition reaction of alkyl or aryl halide, sodi
Copper-polymer nanocomposite: An efficient catalyst for green Huisgen click synthesis
Zuraev, Alexander V.,Grigoriev, Yuri V.,Budevich, Vladislav A.,Ivashkevich, Oleg A.
supporting information, p. 1583 - 1586 (2018/03/23)
A new method for Huisgen [3+2] cycloaddition synthesis of 1,4- and 1,4,5-substituted-1H-1,2,3-triazoles was reported. The reaction was catalyzed by the product of thermolysis of copper (II) poly-5-vinyltetrazolate. Heterogeneous catalyst includes copper nanoparticles which supported on polymeric matrix. It presents recovered and recycled catalyst and the catalyzed reaction proceeds in aerobic conditions at room temperature in aqueous media.