Photoinduced Co-catalyzed dehydrogenative cyclization of 2-alkenylphenyl carbonyl compounds and mechanistic insights

Abstract

In this work, we present a UV-induced 6π-cyclization protocol enabling the synthesis of polysubstituted naphthol skeletons using a single cobaloxime catalyst. In addition, the dual-function photosensitizer 4CzIPN served as both an energy transfer (EnT) photosensitizer and a single electron transfer (SET) photocatalyst within the reaction, leading to the synthesis of the same skeleton under visible light irradiation. The sole by-product of the two strategies was hydrogen, offering potential utility.

Graphical abstract: Photoinduced Co-catalyzed dehydrogenative cyclization of 2-alkenylphenyl carbonyl compounds and mechanistic insights

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Research Article
Submitted
13 Nov 2024
Accepted
07 Jan 2025
First published
08 Jan 2025

Org. Chem. Front., 2025, Advance Article

Photoinduced Co-catalyzed dehydrogenative cyclization of 2-alkenylphenyl carbonyl compounds and mechanistic insights

H. Li, X. Yang, F. Zhou, J. Li, Q. Meng and X. Niu, Org. Chem. Front., 2025, Advance Article , DOI: 10.1039/D4QO02132K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements