Issue 35, 2024

Visible light induced cooperative carbonylation and (hetero)aryl migration: synthesis of multi-carbonyl compounds

Abstract

Carbonylative transformation represents one of the most straightforward procedures for the synthesis of carbonyl-containing compounds. However, the carbonylative procedure toward 1,4-diketones is still limited which are key moieties with potent applications in various areas. Herein, we report a new strategy for the synthesis of multi-carbonyl compounds containing a 1,4-diketone skeleton through remote heteroaryl migration of traditionally restricted 1,3-migratory substrates utilizing carbon monoxide (CO) as the C1 synthon and diazonium compounds as the starting material.

Graphical abstract: Visible light induced cooperative carbonylation and (hetero)aryl migration: synthesis of multi-carbonyl compounds

Supplementary files

Article information

Article type
Edge Article
Submitted
17 May 2024
Accepted
22 Jul 2024
First published
14 Aug 2024
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2024,15, 14304-14309

Visible light induced cooperative carbonylation and (hetero)aryl migration: synthesis of multi-carbonyl compounds

H. Yang, Y. Wang, L. Wang and X. Wu, Chem. Sci., 2024, 15, 14304 DOI: 10.1039/D4SC03221G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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