diastereoisomers

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di·a·ster·e·o·i·so·mers

(dī'ă-ster'ē-ō-ī'sō-merz),
Optically active isomers that are not enantiomorphs (mirror images), for example, d-glucose and d-galactose.
References in periodicals archive ?
Silymarin consists of at least seven flavonolignans, of which the most prevalent are the diastereoisomers silybin A and silybin B; silibinin consists only of silybin A and silybin B.
We were not able to separate the isomers present in the pheromone volatiles collected from females or synthetic stereoisomers with 2 different chiral columns because the enantiomers of branched aliphatic hydrocarbons do not possess a functional group that permits derivatized into diastereoisomers that could be separated by chromatographic methods or by spectroscopic techniques such as Nuclear Magnetic Resonance (Meierhenrich et al.
It is postulated that the glucose a-anomers bind faster than the [beta\-anomers, but the overall response is poor because the relative abundance of [alpha]-anomers is low and interconversion between the different diastereoisomers is slow.
The hydroboration of 7a (diastereomeric mixture) resulted in 6- and 7-hydroxy methylacetals 8a and 9a, as a sum of 8 regio- and diastereoisomers (ratio of 8a and 9a was 4 : 1), and also 4% of the corresponding 6(S)-hydroxylactol 10.
The diastereoisomers of 7b were in the first attempt separated with flash chromatography (eluent 2-5% EtOAc in petroleum ether).
This chip also can be used for polar small molecules and structurally related compounds, such as geometric isomers and diastereoisomers.