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An efficient diastereoselective synthesis of novel fused 5H-furo[2,3-d]thiazolo[3,2-a]pyrimidin-5-ones via one-pot three-component reaction.
Tabibi, Tooba; Esmaeili, Abbas Ali; Mague, Joel T.
Afiliación
  • Tabibi T; Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran.
  • Esmaeili AA; Department of Chemistry, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran. abesmaeili@um.ac.ir.
  • Mague JT; Department of Chemistry, Tulane University, New Orleans, LA, USA.
Mol Divers ; 26(1): 183-190, 2022 Feb.
Article en En | MEDLINE | ID: mdl-33389558
ABSTRACT
Herein, a convenient and efficient synthesis of 7-benzoyl-6-(aryl)-6,7-dihydro-5H-furo[2,3-d]thiazolo[3,2-a]pyrimidin-5-one derivatives was achieved from the reaction of isoquinolinium N-ylides, aromatic aldehydes, and heterocyclic 1,3-dicarbonyl compounds via one-pot three-component diastereoselective domino reaction in good-to-excellent yields. The advantages of this protocol are easily available starting materials, operational simplicity, and avoidance of hazardous organic solvents and catalyst. The synthesized products were characterized by IR, 1H NMR, 13C NMR and mass spectra. Additionally, the conclusive structure of target compounds was confirmed by X-Ray diffraction analysis.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría de Masas Idioma: En Revista: Mol Divers Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Espectrometría de Masas Idioma: En Revista: Mol Divers Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Irán