Reductive Formylation of Nitroarenes Mediated by Rongalite
Overview
Overview
Journal
Org Lett
Publisher
American Chemical Society
Specialties
Biochemistry
Chemistry
Chemistry
Date
2023 Sep 28
PMID
37767992
Authors
Affiliations
Affiliations
Soon will be listed here.
Abstract
Herein, we disclose a straightforward approach to access transition-metal-free reductive -formylation of nitroarenes. This reaction integrates the dual role of rongalite, which acts as a reductant and a C1 building block concurrently. This provides an alternative method for the synthesis of -aryl formamides from nitroarenes, including the construction of a C-N bond. The utility of this protocol was demonstrated by scale-up synthesis and late-stage functionalizations of complex molecules.
Citing Articles
Abbasi F, Sardarian A Sci Rep. 2024; 14(1):7206.
PMID: 38532063 PMC: 10966014. DOI: 10.1038/s41598-024-57608-8.