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作 者:Weiguo Wang Shuai Huang Shikun Yan Xuejun Sun Chen-Ho Tung Zhenghu Xu
机构地区:[1]School of Chemistry and Chemical Engineering,Qufu Normal University,Qufu,Shandong 273165,China [2]Key Lab for Colloid and Interface Chemistry of Education Ministry,Shandong University,Jinan,Shandong 250100,China [3]State Key Laboratory of Organometallic Chemistry,Shanghai Institute of Organic Chemistry,Chinese Academy of Sciences,Shanghai 200032,China
出 处:《Chinese Journal of Chemistry》2020年第5期445-448,共4页中国化学(英文版)
基 金:support from the Natural Science Foundation of China and Shandong Province(Nos.21572118,21971149,ZR2018MB014,ZR2019ZD45);Tang scholar award and the Fundamental Research Funds of Shandong University.
摘 要:Herein,we report a practical protocol for the synthesis of sulfur cycle fused 1,2,3-triazoles through a copper(I)-catalyzed tandem click/intramolecular sulfenylation reaction.The reaction proceeded via a copper-catalyzed alkyne azide cycloaddition,followed by interception of the in situ formed cuprate-triazole intermediate with p-toluenesulfonothioate.This reaction shows broad substrate scope,complete regioselectivity,and excellent functional group tolerance under mild reaction conditions.
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