Title of article
Synthesis of 4H-[1,3]dithiolo[4,5-b]pyrroles through the reaction of benzoyl isothiocyanate and dialkyl acetylenedicarboxylates in the presence of Ph3P
Author/Authors
Yavari، نويسنده , , Issa and Djahaniani، نويسنده , , Hoorieh، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
4
From page
2953
To page
2956
Abstract
Benzoyl isothiocyanate reacts with dialkyl acetylenedicarboxylates in the presence of triphenylphosphine in a mechanistically novel reaction to afford highly substituted dialkyl 2-(benzoylimino)-5-phenyl-4H-[1,3]dithiolo[4,5-b]pyrrole-4,6-dicarboxylates with double insertion of the isothiocyanate. The reaction proceeds via a carbon to nitrogen migration of an alkoxycarbonyl group.
Keywords
oxazine , Acetylenic ester , Benzoyl isothiocyanate , Dithiolopyrrole , Intramolecular Wittig reaction
Journal title
Tetrahedron Letters
Serial Year
2006
Journal title
Tetrahedron Letters
Record number
1849782
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