Separation, by G.L.C., of enantiomeric sugars as diastereoisomeric dithioacetals
Autor: | Little, Mark R. |
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Zdroj: | Carbohydrate Research; July 1982, Vol. 105 Issue: 1 p1-8, 8p |
Abstrakt: | The reaction between (+)-1-phenylethanethiol and each of a pair of enantiomeric sugars produced two acyclic, diastereoisomeric dithioacetals. These diastereomers were then separated by gas-liquid chromatography. This method was applied to separate the following pairs of enantiomers: d- and l-arabinose, d- and l-lyxose, d- and l-fucose, d- and l-rhamnose, d- and l-galactose, d- and l-glucose, and d- and l-mannose. |
Databáze: | Supplemental Index |
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