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An iron(<scp>ii</scp>)-based metalloradical system for intramolecular amination of C(sp<sup>2</sup>)–H and C(sp<sup>3</sup>)–H bonds: synthetic applications and mechanistic studies

Sandip Das, Subrata Das, Supratim Ghosh, Satyajit Roy, Monika Pareek, Brindaban Roy, Raghavan B. Sunoj, Buddhadeb Chattopadhyay

2022Chemical Science55 citationsDOIOpen Access PDF

Abstract

)-H amination reactions involve a metalloradical activation mechanism, which is different from the previously reported electro-cyclization mechanism. Collectively, this study reports the discovery of a new class of metalloradical activation modes using a base metal catalyst that should find wide application in the context of medicinal chemistry, drug discovery and industrial applications.

Topics & Concepts

AminationIntramolecular forceChemistryRegioselectivityTetrazoleCatalysisCombinatorial chemistryPorphyrinAzideContext (archaeology)MoleculeStereochemistryMedicinal chemistryOrganic chemistryBiologyPaleontologySynthesis and Catalytic ReactionsCatalytic C–H Functionalization MethodsCyclopropane Reaction Mechanisms
An iron(<scp>ii</scp>)-based metalloradical system for intramolecular amination of C(sp<sup>2</sup>)–H and C(sp<sup>3</sup>)–H bonds: synthetic applications and mechanistic studies | Litcius