4.7 Article

A copper-catalyzed cascade reaction of o-bromoarylisothiocyanates with isocyanides leading to benzo[d]imidazo[5,1-b]thiazoles under ligand-free conditions

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 3, Issue 5, Pages 556-560

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6qo00030d

Keywords

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Funding

  1. National Natural Science Foundation of China [21302110, 21302109, 21375075]
  2. Scientific Research Foundation of Qufu Normal University [BSQD 2012021]
  3. Taishan Scholar Foundation of Shandong Province
  4. Natural Science Foundation of Shandong Province [ZR2013BQ017]
  5. Shandong Province Higher Educational Science and Technology Program [J13LD14]

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A convenient and efficient copper-catalyzed domino method has been initially developed for the synthesis of benzo[d]imidazo[5,1-b]thiazole derivatives via the reactions of readily available substituted o-bromoarylisothiocyanates with isocyanides under ligand-free conditions. This chemistry involves intermolecular [3 + 2] cycloaddition and intramolecular Ullmann-type C-S bond formation.

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