Efficient and Economical Access to Substituted Benzothiazoles: Copper‐Catalyzed Coupling of 2‐Haloanilides with Metal Sulfides and Subsequent Condensation | Zendy

Ma Dawei | Zendy; Xie Siwei | Zendy; Xue Peng | Zendy; Zhang Xiaojing | Zendy; Dong Jinhua | Zendy; Jiang Yongwen | Zendy

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Efficient and Economical Access to Substituted Benzothiazoles: Copper‐Catalyzed Coupling of 2‐Haloanilides with Metal Sulfides and Subsequent Condensation

Author(s) -

Ma Dawei,

Xie Siwei,

Xue Peng,

Zhang Xiaojing,

Dong Jinhua,

Jiang Yongwen

Publication year - 2009

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.200900486

Subject(s) - condensation , copper , catalysis , metal , coupling (piping) , chemistry , combinatorial chemistry , polymer chemistry , organic chemistry , materials science , metallurgy , physics , thermodynamics

Don′t tell azole : The first metal‐catalyzed direct coupling of metal sulfides with aryl halides and subsequent intramolecular condensation provided substituted benzothiazoles (see scheme). A wide range of functional groups are tolerated under the reaction conditions.

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