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N2-selective alkylation of NH-1,2,3-triazoles with vinyl ethers via gold catalysis.


ABSTRACT: A new method was developed to synthesize N2-alkyl-substituted 1,2,3-triazoles via gold catalyzed alkylation of vinyl ethers with mono- and unsubstituted NH-1,2,3-triazoles and benzotriazole. A hydrogen bond between the oxygen atom of the vinyl ethers, activated via the gold catalyst, and the NH-1,2,3-triazoles was supposed to be generated, which selectively gave the N2-alkylation products.

SUBMITTER: Luo G 

PROVIDER: S-EPMC9083898 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature

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N<sup>2</sup>-selective alkylation of NH-1,2,3-triazoles with vinyl ethers <i>via</i> gold catalysis.

Luo Guoli G   Sun Chenyang C   Li Yan Y   Li Xiaoxiao X   Zhao Zhigang Z  

RSC advances 20180802 49


A new method was developed to synthesize N<sup>2</sup>-alkyl-substituted 1,2,3-triazoles <i>via</i> gold catalyzed alkylation of vinyl ethers with mono- and unsubstituted NH-1,2,3-triazoles and benzotriazole. A hydrogen bond between the oxygen atom of the vinyl ethers, activated <i>via</i> the gold catalyst, and the NH-1,2,3-triazoles was supposed to be generated, which selectively gave the N<sup>2</sup>-alkylation products. ...[more]

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