Access to substituted thiapyrrolizidinones and fused pyridones using the domino N-acyliminium-thionium equilibrium/1,3-dipolar cycloaddition/desulfurization cyclization cascade - Normandie Université Access content directly
Journal Articles Tetrahedron Year : 2006

Access to substituted thiapyrrolizidinones and fused pyridones using the domino N-acyliminium-thionium equilibrium/1,3-dipolar cycloaddition/desulfurization cyclization cascade

Abstract

Substituted thiapyrrolizidinones and fused pyridones, and quinolizinones were reported efficaciously from suitable thioamides in yields ranging from 30% to 65%. The reaction proceeded in a one-pot procedure as cascade process by the intramolecular 1,3-dipolar cycloaddition of thioisomünchnones followed by desulfurization of the adducts. During these investigations, the mechanistic aspects of the process were also discussed.

Dates and versions

hal-02564933 , version 1 (06-05-2020)

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Abdulkareem Hamid, Hassan Oulyadi, Adam Daïch. Access to substituted thiapyrrolizidinones and fused pyridones using the domino N-acyliminium-thionium equilibrium/1,3-dipolar cycloaddition/desulfurization cyclization cascade. Tetrahedron, 2006, 62 (26), pp.6398-6404. ⟨10.1016/j.tet.2006.04.032⟩. ⟨hal-02564933⟩
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