- In stereochemistry,
diastereomers (sometimes
called diastereoisomers) are a type of stereoisomer.
Diastereomers are
defined as non-mirror image, non-identical...
- 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...
-
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)...
-
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...
- direction, the
diastereomer is
referred to as cis,
whereas when the
substituents are
oriented in
opposing directions, the
diastereomer is
referred to...
-
specific enantiomer or
diastereomer.
Enantiomers are
stereoisomers that have
opposite configurations at
every chiral center.
Diastereomers are stereoisomers...
-
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...
- (d-erythro-pentulose) and l-ribulose (l-erythro-pentulose). d-Ribulose is the
diastereomer of d-xylulose.
Ribulose sugars are
composed in the
pentose phosphate...
