- In stereochemistry,
diastereomers (sometimes
called diastereoisomers) are a type of stereoisomer.
Diastereomers are
defined as non-mirror image, non-identical...
- (but not all) centres, they are
diastereomers. All
stereoisomers that are not
enantiomers are
diastereomers.
Diastereomerism also
exists in alkenes. Alkenes...
- 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...
- 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...
- two
enantiomers S,S- and R,R-. The
chiral diastereomers are used in
asymmetric hydrogenation. Both
diastereomers are
bidentate ligands. 1,2-Diphenyl-1,2-ethylenediamine...
- 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)....
-
stereoisomers exist,
enantiomers and
diastereomers.
Enantiomers have
identical physical properties but
diastereomers do not. Two
compounds are said to be...
- (R,S) and (S,S)
diastereomers. (The R-S
notation is
explained here.) The
conversion of the
enantiomeric mixture into a
diastereomer pair,
depending on...
- more
complex compounds.
Diastereomers are non-superposable, non-identical stereoisomers. A
common example of
diastereomerism is when two
compounds differ...
