Abstract
Synthetic studies are reviewed on sugar analogs containing a phosphorus atom in the hemiacetal ring, e.g., analogs of d-xylo, d-gluco, 6-deoxy-l-galacto. d-mannopyranoses, as well as d-ribo and 2-deoxy-d-ribofuranoses. These compounds were converted into the corresponding per-O-acetyl derivatives, whose structures and conformations were established by 1H-NMR spectral analyses and partly by X-ray crystallographic analyses. Stereoselectivity of the introduction of a phosphinyl group to various types of 6-O-tosyl-hex-5-uloses and 6-nitro-hex-5-enoses are also described.
Original language | English |
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Pages (from-to) | 377-387 |
Number of pages | 11 |
Journal | Yuki Gosei Kagaku Kyokaishi/Journal of Synthetic Organic Chemistry |
Volume | 51 |
Issue number | 5 |
DOIs | |
Publication status | Published - 1993 |
Keywords
- Addition of phosphonate
- C-P bond
- Chemical modification of carbohydrate
- Cyclic phosphorus compound
- Phosphoro sugar
ASJC Scopus subject areas
- Organic Chemistry