Photoredox-catalyzed unsymmetrical diamination of alkenes for access to vicinal diamines-Reference-Cited by-同舟云学术

Photoredox-catalyzed unsymmetrical diamination of alkenes for access to vicinal diamines

Published:2024 Issue:25 Volume:60 Page:3413-3416
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Liu Jie¹,Guo Lu²,Chen Zhang¹,Guo Yu¹^ORCID,Zhang Wei¹,Peng Xue¹,Wang Zhen¹³^ORCID,Zeng Yao-Fu¹^ORCID

Affiliation:

1. School of Pharmaceutical Science, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, China

2. Department of Sports Medicine, Affiliated Nanhua Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, China

3. MOE Key Lab of Rare Pediatric Diseases, University of South China, Hengyang, Hunan, 421001, China

Abstract

Unsymmetrical vicinal diamines have been achieved via the photoredox-catalyzed difunctionalization of alkenes by using N-aminopyridinium salts and nitriles as the amination reagents, respectively.

Funder

National Natural Science Foundation of China

Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC00330F

Reference58 articles.

1. Vicinal Diamino Functionalities as Privileged Structural Elements in Biologically Active Compounds and Exploitation of their Synthetic Chemistry

2. Novel pharmacology: asimadoline, a κ-opioid agonist, and visceral sensation

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4. Bepridil is potent against SARS-CoV-2 in vitro

5. α,β-Diamino Acids: Biological Significance and Synthetic Approaches

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