Title of article
A strategy to access fused triazoloquinoline and related nucleoside analogues
Author/Authors
Kapil Upadhyaya، نويسنده , , Arya Ajay، نويسنده , , Rohit Mahar، نويسنده , , Renu Pandey، نويسنده , , Brijesh Kumar، نويسنده , , Sanjeev K. Shukla، نويسنده , , Rama Pati Tripathi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
12
From page
8547
To page
8558
Abstract
Fused triazoloquinolines have been prepared starting from (E)-3-(2-nitrophenyl)-1-aryl-prop-2-en-1-ones and sugar or benzyl azides in a sequential [3+2] cycloaddition reaction, followed by one pot Pd–C assisted reduction, cyclization and aromatization. The triazolyl fused quinolines with N1-glycosyl substituents as unnatural nucleosides have inherent potential to generate a library of compounds for bioevaluations.
Keywords
Cycloaddition , Triazoloquinolines , Reductive cyclization , Unnatural nucleoside
Journal title
Tetrahedron
Serial Year
2013
Journal title
Tetrahedron
Record number
1106291
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