@article{2dd8f8c0622646b79a97cd64f5769f06,
title = "Pd-Catalyzed Etherification of Nitroarenes",
abstract = "The Pd-catalyzed etherification of nitroarenes with arenols has been achieved using a new rationally designed ligand. Mechanistic insights were used to design the ligand so that both the oxidative addition and reductive elimination steps of a plausible catalytic cycle were facilitated. The catalytic system established here provides direct access to a range of unsymmetrical diaryl ethers from nitroarenes.",
author = "Naoki Matsushita and Myuto Kashihara and Michele Formica and Yoshiaki Nakao",
note = "Funding Information: This work was supported by the “JST CREST program Grant Number JPMJCR14L3 in Establishment of Molecular Technology towards the Creation of New Functions”, the “JSPS KAKENHI Grant Number JP15H05799 in Precisely Designed Catalysts with Customized Scaffolding{\textquoteright}, and TOSOH corporation. M.K. is grateful for the Research Fellowship of the Japan Society for the Promotion of Science (JSPS) for Young Scientists. M.F. thanks the JSPS for an International Research Fellowship (Postdoctoral Fellowships for Research in Japan (short-term)). We thank Prof. Dr. Kazuhiko Semba and Dr. Naofumi Hara (Kyoto University) for X-ray crystallographic analyses. Publisher Copyright: {\textcopyright} 2021 American Chemical Society",
year = "2021",
month = jul,
day = "26",
doi = "10.1021/acs.organomet.1c00183",
language = "English",
volume = "40",
pages = "2209--2214",
journal = "Organometallics",
issn = "0276-7333",
publisher = "American Chemical Society",
number = "14",
}