C–C bond cleavage arylation and alkenylation of cyclobutanone oxime ethers <i>via</i> photoredox/nickel catalysis-Reference-Cited by-同舟云学术

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C–C bond cleavage arylation and alkenylation of cyclobutanone oxime ethers via photoredox/nickel catalysis

Published:2024 Issue: Volume: Page:
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Peng Chenglin¹,Tang Yingru¹,Sun Shili¹,Wei Yu¹^ORCID,Zhou Weiji²,Guo Li-Na³^ORCID,Xu Liang¹^ORCID,Liu Shuai²^ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering/State Key Laboratory Incubation Base for Green Processing of Chemical Engineering, Shihezi University, Shihezi, 832003, China

2. Bingtuan Energy Development Institute, Shihezi University, Shihezi, 832003, China

3. School of Chemistry, Xi'an Key Laboratory of Sustainable Energy Material Chemistry, Xi'an Jiaotong University, Xi'an 710049, China

Abstract

A unique strategy for iminyl radical-mediated C–C bond cleavage arylation and alkenylation of cyclobutanone oxime ethers is described.

Funder

Shihezi University

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO01364F

Reference45 articles.

1. Nitrile-containing natural products

2. Nitrile-Containing Pharmaceuticals: Efficacious Roles of the Nitrile Pharmacophore

3. Recent advances of dicyano-based materials in biology and medicine

4. (Poly-cyanoacrylate) nanomedicines for cancer and beyond: Lessons learned

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