- In
carbohydrate chemistry, a pair of
anomers (from Gr**** ἄνω 'up, above' and μέρος 'part') is a pair of near-identical
stereoisomers or diastereomers...
- 2',6,6'-Tetrasubstituted
biphenyls can fit into this
latter category.
Anomerism is an
identity for
single bonded ring
structures where "cis" or "Z" and...
-
material in a
solution due to a
change in
proportion of the two
constituent anomers (i.e. the
interconversion of
their respective stereocenters)
until equilibrium...
- α-Arbutin, is a
glycosylated hydroquinone, and an
anomer of the
naturally occurring arbutin. α-Arbutin is used in the
cosmetic and
pharmaceutical industries...
- same name, but
differ in D and L classification.) They are also not
sugar anomers,
since it is not the
anomeric carbon involved in the stereochemistry. Similarly...
- at the
anomeric carbon are
called anomers. The
anomers of D-glucopyranose are diastereomers, with the beta
anomer having a
hydroxyl (−OH)
group pointing...
- the ring. The
resulting possible pair of
stereoisomers is
called anomers. In the α
anomer, the -OH
substituent on the
anomeric carbon rests on the opposite...
-
which is not
involved in a
glycosidic bond,
could be
either an α- or β-
anomer depending on the bond
direction of the
attached hydroxyl group relative...
-
product will
result which,
owing to the
anomeric effect, is
usually the
alpha anomer. Fischer–Speier
esterification - a more
general reaction where an alcohol...
- midplane. Thus each open-chain
monosaccharide yields two
cyclic isomers (
anomers),
denoted by the
prefixes α- and β-. The
molecule can
change between these...
