- (hydroxyl group) at C(l) has been
converted into an OR
group is
called a
pyranoside. The
pyranose ring is
formed by the
reaction of the
hydroxyl group on...
- However, the enzyme's
cellular role may be to
detoxify non-metabolizable
pyranosides by
acetylating them and
preventing their reentry into the cell. Transacetylase...
-
substituents are destabilizing.
Pyranosides are the most
heavily studied cyclic systems.
Studies of
epoxide migration in
pyranosides and
other cyclic epoxy alcohols...
- Pentagalloylglucose, or more
specificially 1,2,3,4,6-penta-O-galloyl-β-D-glucose, is the
pentagallic acid
ester of glucose. It is a
gallotannin and the...
-
substrate specific nature of the
selectivity and the
overall activity of the
pyranoside can
provide major synthetic difficulties. The
overall specificity of the...
-
protecting groups. That is the
reason why the
hydroxyl group at OH-4 in
pyranosides is unreactive.
Hyperconjugation is
involved when OH-4 is anti-periplanar...
- (1→3)-6-deoxy-
glycero -β- d -
manno -heptopyranosyl-(1→4)-α- l -
rhamno -
pyranoside, a
Tetrasaccharide Subunit of the
Lipopolysaccharide from
Plesimonas shigelloides"...
- a pyranos-3-ulose or a pyranos-2,3-diulose) +
reduced acceptor (2) a
pyranoside +
acceptor ⇌ {\displaystyle \rightleftharpoons } a pyranosid-3-ulose (or...
- "Recent
Advances in the
Conversion of
Carbohydrate Furanosides and
Pyranosides into Carbocycles". Angew. Chem. Int. Ed. 38 (6): 773–777. doi:10...
- Neto; et al. (1993). "An
improved synthesis of 2,3- and 3,4-unsaturated
pyranosides: The use of
microwave energy".
Tetrahedron Letters. 34 (52): 8407–8410...
