Title of article :
Synthesis of quercetin 3-O-β-d-apiofuranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside
Author/Authors :
Zhang، نويسنده , , Yang and Wang، نويسنده , , Kejun and Zhan، نويسنده , , Zhilai and Yang، نويسنده , , Yu and Zhao، نويسنده , , Yimin، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Pages :
4
From page :
3154
To page :
3157
Abstract :
A concise method to construct a unique 2,6-branched trisaccharide was established by regioselective glycosylation of three free hydroxyl groups on a 3-O-protected glucose moiety, and successfully used in the synthesis of quercetin 3-O-β-d-apiofuranosyl-(1→2)-[α-l-rhamnopyranosyl-(1→6)]-β-d-glucopyranoside, a flavonol O-glycoside isolated from glandless cotton seeds which showed notable antidepressant activities.
Keywords :
6-Branched oligosaccharides , Flavonol glycoside , 2 , Antidepressant , regioselective glycosylation
Journal title :
Tetrahedron Letters
Serial Year :
2011
Journal title :
Tetrahedron Letters
Record number :
1878517
Link To Document :
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