C4 Functionalization of the Isoquinoline Core via Oxidative Radical Substitution
Year: 2026
Type: article
Abstract: ABSTRACT In this work, we report a straightforward synthetic procedure that enables the selective functionalization of the C4 position of isoquinoline, followed by subsequent transformations of the resulting products. Although numerous synthetic procedures have been reported for obtaining this relevant class of nitrogen heterocycles, only a few methodologies are available for their functionalization, particularly for modifying the heterocyclic ring. The strategy features an oxidative radical substitution process that generates radicals from readily prepared xanthates. Subsequent transformations of the resulting products demonstrate the synthetic potential to access new compounds.
Source: ChemistrySelect
DOI: 10.1002/slct.73568
Institutions: Universidad Nacional Autónoma de México, University of Nariño
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $3,880
Funder: University of Namibia
Award: G3424849810
OpenAlex ID: W7162778043
