4.4 Article

Regioselective synthesis of pyridoquinolones and pyridocoumarins via molecular iodine-mediated 6-endo-dig electrophilic cylization

Journal

TETRAHEDRON LETTERS
Volume 52, Issue 3, Pages 411-414

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2010.11.066

Keywords

Molecular iodine; Pyridoquinolone; Pyridocoumarin; Sonogashira coupling; 6-endo-dig

Funding

  1. CSIR (New Delhi)
  2. DST (New Delhi)
  3. UGC (New Delhi)

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Angular-pyridoquinolone and pyridocoumarin derivatives have been efficiently synthesized in 60-95% yields by molecular iodine-mediated cyclization of easily available starting materials, 6-(N-propargyl)amino quinolone and coumarin derivatives, in the presence of NaHCO(3). The reaction was carried out at room temperature. (C) 2010 Elsevier Ltd. All rights reserved.

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