Title of article
Thiol addition to protected allyl glycosides: An improved method for the preparation of spacer-arm glycosides
Author/Authors
Paul B. van Seeventer، نويسنده , , Johannes A.L.M. van Dorst، نويسنده , , John F. Siemerink، نويسنده , , Johannis P. Kamerling، نويسنده , , Johannes F.G Vliegenthart، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 1997
Pages
5
From page
369
To page
373
Abstract
A useful method for the preparation of differently functionalized sulfide spacer-arm glycosides is presented. Several protected allyl glycosides were variously elongated via a radical addition reaction with pentanethiol, methyl 3-mercaptopropionate, or 2-mercaptoethanol. The hydroxyl function of protected 3-(2-hydroxyethylthio)propyl glycosides was subsequently transformed into an azide function.
Keywords
3-(2-Azidoethylthio)propyl glycosides , Allyl glycosides , Sulfide spacer-arm , Neoglycoconjugates
Journal title
Carbohydrate Research
Serial Year
1997
Journal title
Carbohydrate Research
Record number
961795
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