@article{22a7194cff37492a88d8b02b72dc5bd5,
title = "Pd-Catalyzed Decarbonylative C−H Coupling of Azoles and Aromatic Esters",
abstract = "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.",
keywords = "C−H coupling, decarbonylation, heteroarenes, nickel, palladium",
author = "Kaoru Matsushita and Ryosuke Takise and Tomoya Hisada and Shin Suzuki and Ryota Isshiki and Kenichiro Itami and Kei Muto and Junichiro Yamaguchi",
note = "Funding Information: This work was supported by JSPS KAKENHI Grant Number JP16H01011, JP16H04148 (to J. Y.), and JP17K14453 (to K.M.), the ERATO program from JST (to K. I.), and a JSPS research fellowship for young scientists (to T. R. and S. S.). Materials Characterization Central Laboratory in Waseda University is acknowledged for HRMS measurement. ITbM is supported by the World Premier International Research Center (WPI) Initiative, Japan. Publisher Copyright: {\textcopyright} 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim",
year = "2018",
month = sep,
day = "4",
doi = "10.1002/asia.201800478",
language = "English",
volume = "13",
pages = "2393--2396",
journal = "Chemistry - An Asian Journal",
issn = "1861-4728",
publisher = "John Wiley and Sons Ltd",
number = "17",
}