Affiliation:
1. College of Sciences, Central South University of Forestry and Technology Changsha Hunan 410004 China
2. School of Chemistry and Chemical Engineering, Inner Mongolia University Hohhot Inner Mongolia 010021 China
Abstract
Comprehensive SummaryAn alkyl radical initiated cyclization/tandem reaction of alkyl bromides and alkyl electrophiles by using potassium metabisulphite (K2S2O5) as a connector is developed for the synthesis of various lactam‐substituted alkyl sulfones. Notably, this process does not require a metal catalyst or metal powder reductant, highlighting its environmentally friendly features. The reaction demonstrates outstanding substrate adaptability and a high tolerance towards diverse functional groups. Furthermore, the biologically active molecules and commercially available drugs with a late‐stage modification are also highly compatible with this transformation. Mechanistic studies revealed that the reaction proceeds through a single‐step process involving intramolecular radical cyclization, "SO2" insertion, and external alkyl incorporation.
Funder
Hunan Provincial Innovation Foundation for Postgraduate
Natural Science Foundation of Hunan Province