- In stereochemistry,
diastereomers (sometimes
called diastereoisomers) are a type of stereoisomer.
Diastereomers are
defined as non-mirror image, non-identical...
-
indicators of the
success of an
asymmetric synthesis. For
mixtures of
diastereomers,
there are
analogous definitions and uses for
diastereomeric excess...
-
optically active compound shows two forms: D-(+) form and L-(−) form.
Diastereomers are
stereoisomers not
related through a
reflection operation. They are...
- not
rotate light.
Stereoisomers include both
enantiomers and
diastereomers.
Diastereomers, like enantiomers,
share the same
molecular formula and are also...
-
specific enantiomer or
diastereomer.
Enantiomers are
stereoisomers that have
opposite configurations at
every chiral center.
Diastereomers are stereoisomers...
-
reaction is one in
which one
diastereomer is
formed in
preference to
another (or in
which a
subset of all
possible diastereomers dominates the
product mixture)...
- example,
tartaric acid has
three distinct isomers, a pair of
diastereomers with one
diastereomer forming two enantiomers. An
element is a
chemical substance...
-
hydroxyl group in this
compound is
placed in an exo position. The endo
diastereomer is
called borneol.
Being chiral,
isoborneol exists as enantiomers. Isoborneol...
-
hydroxyl group in this
compound is
placed in an endo position. The exo
diastereomer is
called isoborneol.
Being chiral,
borneol exists as enantiomers, both...
- 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...
