| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1385165 | Carbohydrate Research | 2008 | 4 Pages |
Abstract
Treatment of methyl 5-deoxy-2,3-O-isopropylidene-5-(benzylsulfonyl)-β-d-ribofuranoside with CBr2F2–KOH/Al2O3 afforded the corresponding olefinic sugar. The methyl- and the isopropyl-analogues in contrast underwent epimerization at C-4 to generate the α-l-lyxo derivatives.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Tarun Kumar Pal, Tanmaya Pathak,