Title of article :
Semi-synthesis of neomangiferin from mangiferin
Author/Authors :
Wei، نويسنده , , Xiong and Liang، نويسنده , , Danlin and Ning، نويسنده , , Maoheng and Wang، نويسنده , , Qing and Meng، نويسنده , , Xiangbao and Li، نويسنده , , Zhongjun، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Pages :
4
From page :
3083
To page :
3086
Abstract :
Neomangiferin, a natural xanthone derivative bearing both O- and C-glucosides, was isolated from the leaves of Gentiana asclepiadea L. and has shown potential anti-diabetic activity. We describe herein the first semi-synthesis of neomangiferin from the natural C-glucoside mangiferin and glucose. The developed synthesis presents a facile protection strategy using Jurd’s method to distinguish the different phenolic hydroxyl groups. Following this strategy, the regioselective protection of 1,3,6-hydroxyl groups was accomplished and neomangiferin was prepared by glycosylation under the phase-transfer catalysis conditions.
Keywords :
Neomangiferin , semi-synthesis , Regioselective protection , glycosylation , carbohydrate
Journal title :
Tetrahedron Letters
Serial Year :
2014
Journal title :
Tetrahedron Letters
Record number :
1889458
Link To Document :
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