- ring. In some
other cases however,
enediols are
stabilized by
flanking carbonyl groups.
These stabilized enediols are
called reductones. Such species...
- reaction. The
product of the
first step is
enediol-enzyme
complex that can
capture CO 2 or O 2. Thus,
enediol-enzyme
complex is the real carboxylase/oxygenase...
- are
reducing sugars,
because they can
tautomerize into
aldoses via an
enediol intermediate, and the
resulting aldehyde group can be oxidised, for example...
-
organic compounds. They are
enediols with a
carbonyl group adjacent to the
enediol group, i.e. RC(OH)=C(OH)-C(O)R. The
enediol structure is
stabilized by...
- on glucose.[citation needed] Holker, J. R. (1955). "Oxidation of Some
Enediols with
Selenium Dioxide". J. Chem. Soc.: 579–580. doi:10.1039/JR9550000574...
- in a
dynamic process with an enol
intermediate (more specifically, an
enediol). This
process is reversible, so
aldoses and
ketoses can be
thought of...
-
Vitamin C (also
known as
ascorbic acid and ascorbate) is a water-soluble
vitamin found in
citrus and
other fruits,
berries and vegetables. It is also a...
- versa, with a
tautomeric enediol as
reaction intermediate.
Ketoses may be
transformed into 3-ketoses, etcetera. The
enediol is also an
intermediate for...
- enzyme's
active site. The
mechanism involves the
intermediate formation of an
enediol. The
relative free
energy of each
ground state and
transition state has...
-
balance between these isomers is formed. This
reaction proceeds via an
enediol:
Glucose is the most
abundant monosaccharide.
Glucose is also the most...
