Carbohydrate Research p. 1 - 8 (1982)
Update date:2022-08-03
Topics:
Little, Mark R.
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-lyxose, D- and L-fucose, D- and L-rhamnose,D- and L-arabinose, D-and L-galactose, D- andL-glucose, and D- and L-mannose.
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Doi:10.1002/hlca.19820650306
(1982)Doi:10.1016/S0022-328X(00)81213-9
(1982)Doi:10.1246/cl.1982.881
(1982)Doi:10.1016/S0040-4039(00)77153-X
(1994)Doi:10.1021/op010204f
(2001)Doi:10.1021/ic00142a018
(1982)
