- In stereochemistry,
mutarotation is the
change in
optical rotation of a
chiral material in a
solution due to a
change in
proportion of the two constituent...
-
yield the 4-fold
ester α-D-glucofuranose-1,2:3,5-bis(p-tolylboronate).
Mutarotation consists of a
temporary reversal of the ring-forming reaction, resulting...
- an l-configuration furanose. Typically, the
anomeric carbon undergoes mutarotation in solution, and the
result is an
equilibrium mixture of α and β configurations...
-
anomer to the other. For
reducing sugars,
anomerization is
referred to as
mutarotation and
occurs readily in
solution and is
catalyzed by acid and base. This...
- The
molecule can
change between these two
forms by a
process called mutarotation, that
consists in a
reversal of the ring-forming
reaction followed by...
-
glycosidic bond.[citation needed]
Maltose in
aqueous solution exhibits mutarotation,
because the α and β
isomers that are
formed by the
different conformations...
- and then
closing in the
opposite configuration. This
process is
called mutarotation.
Although all
hexoses have
similar structures and
share some general...
-
however he
lacked noting the
importance of
hydrogen ion
concentration and
mutarotation of glucose. The goal of Henri's
thesis was to
compare his
knowledge of...
- pp. 1–67. ISBN 978-0323138338.
Pigman W, Anet EF (1972). "Chapter 4:
Mutarotations and
Actions of
Acids and Bases". In
Pigman W,
Horton D (eds.). The Carbohydrates:...
- of
carbohydrates General Aldose Ketose Furanose Pyranose Geometry Anomer Cyclohexane conformation Epimer Mutarotation Monosaccharides Multiple Category...
