4.7 Article

Catalytic synthesis of functionalized amidines via cobalt-carbene radical coupling with isocyanides and amines

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 8, Issue 7, Pages 1544-1550

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1qo00063b

Keywords

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Funding

  1. NSFC [22001226, 21772208]
  2. Natural Science Foundation of Jiangsu Province [BK20201183]
  3. Key Research Program of Frontier Sciences of CAS [QYZDJSSW-SLH051]
  4. Natural Science Foundation of the Jiangsu Higher Education Institutions of China [20KJB150016, 19KJB150040]
  5. Funding for School-Level Research Projects of Yancheng Institute of Technology [xjr2019032, xjr2019033]

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This method utilizes amines, isocyanides, and diazo compounds as carbene sources to provide a synthetic simple and highly efficient strategy for the straightforward synthesis of functionalized amidines with a range of substrates.
An atom- and step-economic multi-component cobalt-catalyzed synthesis of amidines has been reported by using amines, isocyanides, and diazo compounds as carbene sources. This protocol provides a synthetically simple, highly efficient strategy for the straightforward synthesis of functionalized amidines with a range of substrates.

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