Product selective reaction controlled by the combination of palladium nanoparticles, continuous microwave irradiation, and a co-existing solid; ligand-free Buchwald–Hartwig amination vs. aryne amination-Reference-Cited by-同舟云学术

Product selective reaction controlled by the combination of palladium nanoparticles, continuous microwave irradiation, and a co-existing solid; ligand-free Buchwald–Hartwig amination vs. aryne amination

Published:2021 Issue:20 Volume:23 Page:8131-8137
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Yamada Makito¹^ORCID,Ohta Ryousuke¹,Harada Kazuo¹^ORCID,Takehara Tsunayoshi²^ORCID,Haneoka Hitoshi²,Murakami Yosuke²,Suzuki Takeyuki²^ORCID,Ohki Yuuta³,Takahashi Naoyuki³,Akiyama Toshiki¹^ORCID,Sirimangkalakitti Natchanun¹^ORCID,Sako Makoto¹^ORCID,Murai Kenichi¹^ORCID,Arai Masayoshi¹^ORCID,Arisawa Mitsuhiro¹^ORCID

Affiliation:

1. Graduate School of Pharmaceutical Sciences, Osaka University, Yamada-oka 1-6, Suita, Osaka 565-0871, Japan

2. Comprehensive Analysis Centre, SANKEN (The Institute of Scientific and Industrial Research), Osaka University, Mihogaoka 8-1, Ibaraki, Osaka 567-0047, Japan

3. Tokyo Rikakikai Co. Ltd (Brand: EYELA), TN Koishikawa Bldg. 1-15-17 Koishikawa Bunkyo-ku, Tokyo 112-0002, Japan

Abstract

We have developed a continuous microwave irradiation-assisted Buchwald–Hartwig amination using our original Pd nanoparticle catalyst with a copper plate as a co-existing metal solid.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D1GC01782A

Reference49 articles.

1. The Buchwald–Hartwig Amination After 25 Years

2. PALLADIUM-CATALYZED AROMATIC AMINATION OF ARYL BROMIDES WITHN,N-DI-ETHYLAMINO-TRIBUTYLTIN

3. A Simple Catalytic Method for the Conversion of Aryl Bromides to Arylamines

4. Palladium-catalyzed synthesis of arylamines from aryl halides. Mechanistic studies lead to coupling in the absence of tin reagents

5. Ueber Synthesen in der Biphenylreihe

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