4.5 Article

Copper(II) Triflate Promoted One-Pot Synthesis of Coumarin-, Quinolone-, and Naphthalene-Annulated 2-Aminothiazoles under Ligand-Free Conditions

Journal

SYNTHESIS-STUTTGART
Volume 44, Issue 1, Pages 87-92

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0031-1289608

Keywords

copper triflate; multicomponent reaction; naphthothiazole; domino synthesis; carbon disulfide

Funding

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

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An efficient synthesis of new 2-aminothiazole-annulated compounds is described via copper(II) triflate promoted sequential condensation, arylation, and heterocyclization reactions in one step. The reaction is compatible with a variety of substrates providing efficient access to many biologically important skeletons in good yields.

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