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A solvent-free mechanochemical electrophilic C–H thiocyanation of indoles and imidazo[1,2- <i>a</i> ]pyridines using a cost-effective combination of <i>N</i> -chlorosuccinimide-NaSCN and tandem C–C and C–S bond formation

Soumik Saha, Abigail B. Pinheiro, Amrita Chatterjee, Zigmee T. Bhutia, Mainak Banerjee

2024Green Chemistry26 citationsDOIOpen Access PDF

Abstract

Herein, we demonstrate a solvent-free and cost-effective mechanochemical electrophilic thiocyanation of indoles and imidazo[1,2- a ]pyridines and tandem double C–H activation leading to the formation of C-2 aryl and C-3 thiocyano indoles in a mixer-mill.

Topics & Concepts

TandemElectrophileChemistryArylMedicinal chemistryDouble bondCombinatorial chemistrySolventOrganic chemistryCatalysisAlkylMaterials scienceComposite materialSulfur-Based Synthesis TechniquesCatalytic C–H Functionalization MethodsSynthesis and Catalytic Reactions
A solvent-free mechanochemical electrophilic C–H thiocyanation of indoles and imidazo[1,2- <i>a</i> ]pyridines using a cost-effective combination of <i>N</i> -chlorosuccinimide-NaSCN and tandem C–C and C–S bond formation | Litcius