Glycosyl trichloroacetylcarbamate: a new glycosyl donor for O-glycosylation
Glycosyl trichloroacetylcarbamates, readily obtained by reacting 1-hydroxy sugars with trichloroacetylisocyanate, have been found as excellent glycosyl donors, and the corresponding O-glycosides are formed in good to excellent yields with a fairly good degree of selectivity.
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| Veröffentlicht in: | Carbohydrate research 2005-12, Vol.340 (17), p.2688-2692 |
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| container_title | Carbohydrate research |
| container_volume | 340 |
| creator | Jayakanthan, K. Vankar, Yashwant D. |
| description | Glycosyl trichloroacetylcarbamates, readily obtained by reacting 1-hydroxy sugars with trichloroacetylisocyanate, have been found as excellent glycosyl donors, and the corresponding
O-glycosides are formed in good to excellent yields with a fairly good degree of selectivity. |
| doi_str_mv | 10.1016/j.carres.2005.07.024 |
| format | Article |
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| fulltext | fulltext |
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| ispartof | Carbohydrate research, 2005-12, Vol.340 (17), p.2688-2692 |
| issn | 0008-6215 1873-426X |
| language | eng |
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| source | MEDLINE; Elsevier ScienceDirect Journals |
| subjects | Carbamates - chemistry Carbohydrate Conformation Glycosides - chemical synthesis Glycosides - chemistry Glycosylation Indicators and Reagents Kinetics Models, Molecular O-glycosylation Sugar Alcohols - chemistry Trichloroacetylcarbamate Trichloroacetylisocyanate Trimethylsilyltriflate |
| title | Glycosyl trichloroacetylcarbamate: a new glycosyl donor for O-glycosylation |
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