Title of article
Addressing the scope of the azide–nitrile cycloaddition in glycoconjugate chemistry. The assembly of C-glycoclusters on a calix[4]arene scaffold through tetrazole spacers
Author/Authors
Alessandro Dondoni، نويسنده , , Alberto Marra، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2007
Pages
7
From page
6339
To page
6345
Abstract
New glycoclusters constituted of ribosylmethyl, galactosylmethyl, and glucosylmethyl fragments assembled on a calix[4]arene platform by means of propoxytetrazole spacers have been prepared by coupling the corresponding sugar azides with p-toluenesulfonyl cyanide, and then reacting 1-glycosylmethyl-5-sulfonyl-tetrazole derivatives thus formed with a calix[4]arene tetrol.
Keywords
Glycocluster , 1 , 3-dipolar cycloaddition , Sugar azide , Tetrazole , C-Glycoside
Journal title
Tetrahedron
Serial Year
2007
Journal title
Tetrahedron
Record number
1091106
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