- In stereochemistry,
diastereomers (sometimes
called diastereoisomers) are a type of stereoisomer.
Diastereomers are
defined as non-mirror image, non-identical...
-
specific enantiomer or
diastereomer.
Enantiomers are
stereoisomers that have
opposite configurations at
every chiral center.
Diastereomers are stereoisomers...
-
indicators of the
success of an
asymmetric synthesis. For
mixtures of
diastereomers,
there are
analogous definitions and uses for
diastereomeric excess...
-
equal to the
amount of its enantiomer's
rotation in the (–) direction.
Diastereomers are
stereoisomers not
related through a
reflection operation. They are...
-
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)...
- dl-α-tocopherol). The
mixture of all
eight diastereomers is
called all-rac-α-tocopherol. The α-Tocopherol is the most
active diastereomer biologically,
while being maintained...
- not
rotate light.
Stereoisomers include both
enantiomers and
diastereomers.
Diastereomers, like enantiomers,
share the same
molecular formula and are also...
-
hydroxyl group in this
compound is
placed in an endo position. The exo
diastereomer is
called isoborneol.
Being chiral,
borneol exists as enantiomers, both...
-
chiral centres differ in all of
those centres, they are enantiomers.
Diastereomers are
distinct molecular configurations that are a
broader category. They...
-
antiarrhythmic agent used to
treat heart rhythm disturbances. It is a
diastereomer of
antimalarial agent quinine,
originally derived from the bark of the...
