Photoredox-enabled ring-opening of cyclobutanes <i>via</i> the formation of a carbon radical-Reference-Cited by-同舟云学术

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Photoredox-enabled ring-opening of cyclobutanes via the formation of a carbon radical

Published:2024 Issue:17 Volume:11 Page:4663-4670
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhao Chunhang¹,Ma Wenjing¹,Liu Kairui¹,Xu Ruoyang¹,Ma Xiuya¹,Zhang Yan¹^ORCID

Affiliation:

1. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, and Drug Discovery & Innovation Center, College of Chemistry and Materials Science, Zhejiang Normal University, Jinhua, China

Abstract

The high strain energy of cyclobutanes has been utilized for selective ring-opening, enabling the synthesis of valuable linear aliphatic compounds.

Funder

Natural Science Foundation of Zhejiang Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00996G

Reference90 articles.

1. The Application of Cyclobutane Derivatives in Organic Synthesis

2. Mercurinium ion mediated ring expansion of 1- alkenyl-1-cycloalkanols

3. The kinetics and mechanism of ring opening of radicals containing the cyclobutylcarbinyl system

4. Towards click chemistry: Multicomponent reactions via combinations of name reactions

5. The Enzymology of Organic Transformations: A Survey of Name Reactions in Biological Systems

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