diastereomers

diastereomers have different physical and chemical properties, making them separable by conventional methods.

the reaction produced a pair of diastereomers in unequal amounts.

diastereomers can be separated using column chromatography due to their distinct polarities.

the diastereomeric ratio was determined by nmr spectroscopy.

these diastereomers exhibit significant differences in their biological activity.

the diastereomeric excess reached 95% after optimization of the reaction conditions.

diastereomers are stereoisomers that are not mirror images of each other.

the synthesis yielded diastereomers with different stereochemistry at two chiral centers.

diastereomers can interconvert only if the activation energy barrier is overcome.

the separation of diastereomers is often easier than the separation of enantiomers.

diastereomeric salts were employed to resolve the racemic mixture.

the configuration of diastereomers affects their stability and reactivity significantly.