4.7 Article

C-H Functionalization of Enamides: Synthesis of β-Amidovinyl Sulfones via Visible-Light Photoredox Catalysis

Journal

ADVANCED SYNTHESIS & CATALYSIS
Volume 355, Issue 4, Pages 809-813

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.201200874

Keywords

beta-amidovinyl sulfones; C-H activation; iridium; photochemistry; redox chemistry

Funding

  1. National Basic Research Program of China [2011CB935800]
  2. National Natural Science Foundation of China [2112109, 21102072]
  3. Natural Science Foundation of Jiangsu Province [BK2012012]
  4. State Key Laboratory of Bioorganic & Natural Products Chemistry, Shanghai Institute of Organic Chemistry, CAS

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A mild, practical and environmentally friendly strategy to prepare -amidovinyl sulfones has been developed based on the sulfonation of enamides or enecarbamates via visible-light photoredox catalysis. Direct CH functionalizations of enamides or enecarbamates under the optimized conditions proceeded with a wide scope of substrates and remarkable selectivity to give functionalized vinyl sulfones with good to excellent yields.

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