Pd‐Catalyzed Decarbonylative C−H Coupling of Azoles and Aromatic Esters | Zendy

Matsushita Kaoru | Zendy; Takise Ryosuke | Zendy; Hisada Tomoya | Zendy; Suzuki Shin | Zendy; Isshiki Ryota | Zendy; Itami Kenichiro | Zendy; Muto Kei | Zendy; Yamaguchi Junichiro | Zendy

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Pd‐Catalyzed Decarbonylative C−H Coupling of Azoles and Aromatic Esters

Author(s) -

Matsushita Kaoru,

Takise Ryosuke,

Hisada Tomoya,

Suzuki Shin,

Isshiki Ryota,

Itami Kenichiro,

Muto Kei,

Yamaguchi Junichiro

Publication year - 2018

Publication title -

chemistry – an asian journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.18

H-Index - 106

eISSN - 1861-471X

pISSN - 1861-4728

DOI - 10.1002/asia.201800478

Subject(s) - catalysis , palladium , substrate (aquarium) , chemistry , nickel , scope (computer science) , coupling (piping) , combinatorial chemistry , organic chemistry , materials science , computer science , oceanography , metallurgy , programming language , geology

A decarbonylative C−H coupling of azoles and aromatic esters by palladium catalysis is described. Our previously reported Ni‐catalyzed C−H coupling of azoles and aromatic esters has a significant drawback regarding the substrate scope. Herein, we employ palladium catalysis instead of nickel, resulting in a broader substrate scope in terms of azoles and aromatic esters.

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