@article{54f11d5075714c01882e76b95c626d1c,
title = "Palladium-Catalyzed Mizoroki-Heck Reaction of Nitroarenes and Styrene Derivatives",
abstract = "We have developed a Mizoroki-Heck reaction of nitroarenes with alkenes under palladium catalysis. The use of a Pd/BrettPhos catalyst promoted the alkenylation, whereas other catalysts led to a decrease in the product yield. In addition to nitroarenes, nitroheteroarenes were also applicable to the present reaction. The combination of a nucleophilic aromatic substitution (SNAr) with the denitrative alkenylation produced a multifunctionalized arene in a one-pot operation.",
author = "Toshimasa Okita and Asahara, {Kitty K.} and Kei Muto and Junichiro Yamaguchi",
note = "Funding Information: This work was supported by JSPS KAKENHI Grant Number JP19H02726 (to J.Y.), JP18H04661 (Hybrid Catalysis), and JP19K15573 (to K.M.). We thank Kaoru Matsushita and Tomoya Hisada (Waseda University) for initial experiments. We also thank Prof. Yoshiaki Nakao (Kyoto University) for providing NHC ligands. The Materials Characterization Central Laboratory in Waseda University is acknowledged for the support of HRMS measurements. Publisher Copyright: Copyright {\textcopyright} 2020 American Chemical Society.",
year = "2020",
month = apr,
day = "17",
doi = "10.1021/acs.orglett.0c00983",
language = "English",
volume = "22",
pages = "3205--3208",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "8",
}