Reductive C(sp3)–C(sp3) homo-coupling of benzyl or allyl halides with H2 using a water-soluble electron storage catalyst-Reference-Cited by-同舟云学术

Reductive C(sp3)–C(sp3) homo-coupling of benzyl or allyl halides with H2 using a water-soluble electron storage catalyst

Published:2021 Issue:62 Volume:11 Page:39450-39454
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Yatabe Takeshi¹²³,Futakuchi Sayaka¹,Miyazawa Keishi¹,Shimauchi Daiki¹,Takahashi Yukina¹²,Yoon Ki-Seok¹²³,Nakai Hidetaka⁴^ORCID,Ogo Seiji¹²³^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, Graduate School of Engineering, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan

2. International Institute for Carbon-Neutral Energy Research (WPI-I2CNER), Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan

3. Center for Small Molecule Energy, Kyushu University, 744 Moto-oka, Nishi-ku, Fukuoka 819-0395, Japan

4. Department of Applied Chemistry, Faculty of Science and Engineering, Kindai University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan

Abstract

Four requirements for the reductive C(sp3)–C(sp3) homo-coupling of benzyl/allyl halides in aqueous solution by using H2 as an electron source are described.

Funder

Core Research for Evolutional Science and Technology

Japan Society for the Promotion of Science

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/RA/D1RA08596D

Reference47 articles.

1. Reductive Cross-Coupling Reactions between Two Electrophiles

2. Methods and Mechanisms for Cross-Electrophile Coupling of Csp2 Halides with Alkyl Electrophiles

3. An anodic aromatic C,C cross-coupling reaction using parallel laminar flow mode in a flow microreactor

4. Metal-catalyzed reductive coupling of olefin-derived nucleophiles: Reinventing carbonyl addition

5. Nickel/Cobalt-Catalyzed C(sp3)–C(sp3) Cross-Coupling of Alkyl Halides with Alkyl Tosylates

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