960化工网
Dicarbofunctionalization of unactivated alkenes via organo-photoredox catalysis in water: access to cyanoalkylated fused quinazolinones†
Organic & Biomolecular Chemistry Pub Date : 06/12/2023 00:00:00 , DOI:10.1039/D3OB00716B
Abstract

A visible light-induced C–C bond cleavage/addition/cyclization cascade of oxime esters and unactivated alkenes has been developed using water as the solvent. This green protocol offers an easy access to medicinally valuable cyanoalkylated quinazolinones. Mild reaction conditions, functional group tolerance and late-stage functionalization of complex molecules are the important features of this transformation.

Graphical abstract: Dicarbofunctionalization of unactivated alkenes via organo-photoredox catalysis in water: access to cyanoalkylated fused quinazolinones
平台客服
平台客服
平台在线客服