General synthesis of secondary imines <i>via</i> reductive coupling of carbonyl and nitro compounds employing a reusable cobalt catalyst-Reference-Cited by-同舟云学术

General synthesis of secondary imines via reductive coupling of carbonyl and nitro compounds employing a reusable cobalt catalyst

Published:2024 Issue:4 Volume:9 Page:925-929
ISSN:2058-9883
Container-title:Reaction Chemistry & Engineering
language:en
Short-container-title:React. Chem. Eng.

Author:

Zhang Chaochong¹,He Yurong¹,Zhou Peng¹^ORCID,Ma Yuandie¹,Yuan Ziliang¹,She Guoqiang¹,Zheng Zhe¹,Hu Juncheng¹^ORCID,Jiang Qingqing¹^ORCID,Lam Jason Chun-Ho¹^ORCID,Han Bo¹^ORCID,Zhang Zehui¹^ORCID,Liu Bing¹^ORCID

Affiliation:

1. Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, College of Chemistry and Material Science, South-Central Minzu University, Wuhan, 430074, People's Republic of China

Abstract

Reusable nitrogen-doped carbon-encapsulated Co nanoparticle catalysts are found robust for the synthesis of secondary imines via the reductive amination of carbonyl compounds with NH3 or directly with nitro compounds.

Funder

Natural Science Foundation of Hubei Province

National Natural Science Foundation of China

Fundamental Research Funds for the Central Universities

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/RE/D3RE00509G

Reference29 articles.

1. Nickel-catalyzed hydrogenative coupling of nitriles and amines for general amine synthesis

2. Direct access to chiral aliphatic amines by catalytic enantioconvergent redox-neutral amination of alcohols

3. MOF-derived cobalt nanoparticles catalyze a general synthesis of amines

4. Transition-Metal-Catalyzed Reductive Amination Employing Hydrogen

5. Reductive Amination in the Synthesis of Pharmaceuticals