4.5 Article

Tandem Reactions Leading to Benzo[c]chromen-6-ones and 3-Substituted Isocoumarins

Journal

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
Volume 2012, Issue 4, Pages 673-677

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201101559

Keywords

Natural products; Fused-ring systems; Copper; Domino reactions

Funding

  1. National Natural Science Foundation of China [20972042, 20911140238]
  2. Innovation Scientists and Technicians Troop Construction Projects of Henan Province [104100510019]
  3. Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT) [IRT1061]

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A simple and convenient protocol for the synthesis of benzo[c]chromen-6-ones and 3-substituted isocoumarins through a CuI-catalyzed tandem reaction of 2-bromobenzoates withcyclohexane-1,3-diones or acyclic 1,3-diones is developed. This strategy can also be extended to the one-pot synthesis of isoquinolin-1(2H)-one and 3,4-dihydrophenanthridine-1,6(2H,5H)-dione.

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