- In stereochemistry,
diastereomers (sometimes
called diastereoisomers) are a type of stereoisomer.
Diastereomers are
defined as non-mirror image, non-identical...
-
optically active compound shows two forms: D-(+) form and L-(−) form.
Diastereomers are
stereoisomers not
related through a
reflection operation. They are...
- (but not all) centres, they are
diastereomers. All
stereoisomers that are not
enantiomers are
diastereomers.
Diastereomerism also
exists in alkenes. Alkenes...
- as are (R,S) and (S,R).
Diastereomers have at
least one
descriptor in common; for
example (R,S) and (R,R) are
diastereomers, as are (S,R) and (S,S)....
- not
rotate light.
Stereoisomers include both
enantiomers and
diastereomers.
Diastereomers, like enantiomers,
share the same
molecular formula and are also...
- In stereochemistry, an
epimer is one of a pair of
diastereomers. The two
epimers have
opposite configuration at only one
stereogenic center out of at...
- but can
distinguish diastereomers. Therefore,
converting a
mixture of
enantiomers to a
corresponding mixture of
diastereomers can
allow analysis. The...
- above' and μέρος 'part') is a pair of near-identical
stereoisomers or
diastereomers that
differ at only the
anomeric carbon, the
carbon atom that bears...
- 5-Dimethylpiperidines are
chemical compounds with the
formula C5H8(CH3)2NH. Two
diastereomers exist: the
achiral R,S
isomer and the
chiral R,R/S,S
enantiomeric pair...
-
specific enantiomer or
diastereomer.
Enantiomers are
stereoisomers that have
opposite configurations at
every chiral center.
Diastereomers are stereoisomers...
