@article{fb46499640304cad8980bae33ad7259e,
title = "Decarbonylative Reductive Coupling of Aromatic Esters by Nickel and Palladium Catalyst",
abstract = "Ni or Pd-catalyzed decarbonylative reductive couplings of aromatic esters were developed. A range of (hetero)aromatic esters was applicable to these reductive homocoupling reactions. Moreover, it was found that Pd-catalysis enables a reductive decarbonylative cross-coupling between two different aromatic esters to afford a nonsymmetrical biaryls system.",
keywords = "Biaryls, Decarbonylative reaction, Reductive coupling",
author = "Yunfei Peng and Ryota Isshiki and Kei Muto and Junichiro Yamaguchi",
note = "Funding Information: This work was supported by JSPS KAKENHI Grant Number JP21H05213 (to J.Y.), JP21K05079 (to K.M.) and JP19J23053 (to R.I.). This work was also partly supported by JST ERATO Grant Number JPMJER1901 (to J.Y.). The Materials Characterization Central Laboratory at Waseda University is acknowledged for the support of HRMS measurement. We also would like to thank National Institute of Health Sciences in Japan for the support of NMR measurement. Publisher Copyright: {\textcopyright} 2022 The Chemical Society of Japan.",
year = "2022",
month = jul,
doi = "10.1246/cl.220214",
language = "English",
volume = "51",
pages = "749--753",
journal = "Chemistry Letters",
issn = "0366-7022",
publisher = "Chemical Society of Japan",
number = "7",
}