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Remote Directed Isocyanation of Unactivated C(sp<sup>3</sup>)–H Bonds: Forging Seven-Membered Cyclic Ureas Enabled by Copper Catalysis

Hongwei Zhang, Peiyuan Tian, Lishuang Ma, Yulu Zhou, Cuiyu Jiang, Xufeng Lin, Xiao Xiao

2020Organic Letters41 citationsDOI

Abstract

Reported herein is an unprecedented copper-catalyzed site-selective δ-C(sp3)–H bonds activation of aliphatic sulfonamides for constructing the synthetically useful seven-membered N-heterocycles. A key to success is the use of in-situ-formed amide radicals, to activate the inert C(sp3)–H bond, and inexpensive TMSNCO, as a coupling reagent under mild conditions. To the best of our knowledge, this represents the first use of alkylamine derivatives as a five-membered synthon to prepare a seven-membered N-heterocycles.

Topics & Concepts

ChemistrySynthonCatalysisReagentAmideCopperRadicalCombinatorial chemistryMedicinal chemistryOrganic chemistryCatalytic C–H Functionalization MethodsSulfur-Based Synthesis TechniquesSynthesis and Catalytic Reactions
Remote Directed Isocyanation of Unactivated C(sp<sup>3</sup>)–H Bonds: Forging Seven-Membered Cyclic Ureas Enabled by Copper Catalysis | Litcius