Chemistry:L-Streptose
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Revision as of 02:08, 10 April 2021 by imported>Corlink (add)
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IUPAC name
5-Deoxy-3-C-formyl-α-l-lyxofuranose
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3D model (JSmol)
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PubChem CID
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Properties | |
C6H10O5 | |
Molar mass | 162.141 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
l-Streptose is a branched monosaccharide similar to apiose in structure. l-Streptose is one of the sugars in streptomycin, an aminoglycoside antibiotic that has toxic effects in the kidney and other side effects.
l-Streptose has been prepared from a carbohydrate derivative.[1] The protected monosaccharide was reacted with an organolithium sulfur compound and then catalytically hydrolyzed to produce l-streptose.
References
- ↑ Block E. "Organic Chemistry: Reactions of Organosulfur Compounds", vol. 37, page 71.
Original source: https://en.wikipedia.org/wiki/L-Streptose.
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