| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1390989 | Carbohydrate Research | 2006 | 9 Pages |
Abstract
Glycosylation of various glycosyl acceptors with 2′-carboxybenzyl (CB) 2,3,4,6-tetra-O-benzyl-β-d-glucopyranoside and CB 2,3,4,6-tetra-O-benzyl-α-d-mannopyranoside as glycosyl donors afforded α-C-glycosides exclusively or predominantly in good yields. CB glycosides were also converted to other well-known glycosyl donors, the corresponding phenyl thioglycoside and the glycosyl fluoride derivatives.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yong Joo Lee, Ju Yuel Baek, Bo-Young Lee, Sung Soo Kang, Hye-Seo Park, Heung Bae Jeon, Kwan Soo Kim,
