Base‐Promoted Regiospecific Synthesis of Fully Substituted 1,2,3‐Triazoles and 1,5‐Disubstituted 1,2,3‐Triazoles | Zendy

Zhang Xueying | Zendy; Cui Xue | Zendy; Wang Wei | Zendy; Zeng Tingting | Zendy; Wang Yan | Zendy; Tan Yinfeng | Zendy; Liu Dongyan | Zendy; Wang Xuesong | Zendy; Li Youbin | Zendy

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Base‐Promoted Regiospecific Synthesis of Fully Substituted 1,2,3‐Triazoles and 1,5‐Disubstituted 1,2,3‐Triazoles

Author(s) -

Zhang Xueying,

Cui Xue,

Wang Wei,

Zeng Tingting,

Wang Yan,

Tan Yinfeng,

Liu Dongyan,

Wang Xuesong,

Li Youbin

Publication year - 2020

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.202000479

Subject(s) - chemistry , diazo , cleavage (geology) , combinatorial chemistry , bond cleavage , stereochemistry , substrate (aquarium) , medicinal chemistry , catalysis , organic chemistry , oceanography , geotechnical engineering , fracture (geology) , engineering , geology

An efficient strategy have been developed for the synthesis of fully substituted 1,2,3‐triazoles and 1,5‐disubstituted 1,2,3‐triazoles subsequently by C−C bond cleavage. Regitz diazo‐transfer and C−C bond cleavage process were involved in this reaction to give 1,2,3‐triazoles with good substrate tolerance. This protocol provideed a facile and an expeditious approach for the assembly of diversely structural 1,2,3‐triazoles.

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