| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5272329 | Tetrahedron Letters | 2009 | 4 Pages |
Abstract
A new sialyl donor, N,N-acetyl, benzoyl-O-perbenzoyl-protected p-toluenethiosialoside, was synthesized and its sialylation reaction was investigated. This reaction proceeded in dichloromethane and β anomeric selectivity was achieved when NIS-TfOH was used as promoter. This method may be employed to construct the unnatural β-linked sialosides.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yue Wang, Xin-Shan Ye,