4.8 Article

Transition-Metal-Assisted Radical/Radical Cross-Coupling: A New Strategy to the Oxidative C(sp3)-H/N-H Cross-Coupling

期刊

ORGANIC LETTERS
卷 16, 期 12, 页码 3404-3407

出版社

AMER CHEMICAL SOC
DOI: 10.1021/ol501485f

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资金

  1. 973 Program [2012CB725302]
  2. National Natural Science Foundation of China [21390400, 21025206, 21272180, 21302148, 21372266, 51302327]
  3. Research Fund for the Doctoral Program of Higher Education of China [20120141130002]
  4. Program for Changjiang Scholars and Innovative Research Team in University [IRT1030]

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A transition-metal-assisted oxidative C(sp(3))-H/N-H cross-coupling reaction of N-alkoxyamides with aliphatic hydrocarbons is described. During the reaction, nitrogen radicals were generated from the oxidation of N-alkoxyamides. Experiments and DFT calculations revealed that transition-metal catalyst could lower the reactivity of the generated nitrogen radical by the coordination of the transition metal, which allowed the selective radical/radical cross-coupling with the transient sp(3) carbon radical to construct C(sp(3))--N bonds. Various C(sp(3))-H bonds could be transformed into C(sp(3))-N bonds through this radical amidation strategy.

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