Examples of 'anomeric' in a sentence
Meaning of "anomeric"
Anomeric: relating to the configuration of a carbon atom in a cyclic form of a saccharide, particularly referring to the anomeric carbon that determines the alpha or beta orientation of the molecule
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- Relating to or characteristic of an anomer
- Synonym of anomer
How to use "anomeric" in a sentence
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anomeric
Through this reaction an anomeric centre is created.
Different anomeric forms of sugars are also encompassed.
This is consistent with the anomeric effect stabilization.
Anomeric carbon atom of the sugar.
It is removed when it is desired to activate the anomeric carbon.
Anomeric mixtures are expressed as a percent.
Several explanations for the anomeric effect have been proposed.
This characteristic avoids a stereoselective synthesis of the anomeric center.
Acute coalescent anomeric coliosis.
The anomeric hydroxyl group is protected with acetic anhydride in pyridine.
Cyclic sugars show mutarotation as α and β anomeric forms interconvert.
It is an anomeric deacetylation.
It adopts a double displacement mechanism with retention of anomeric configuration.
The same anomeric ratio of unprotected nucleoside is obtained by removal of protecting groups.
Permethylation of monosaccharides yields mixtures of anomeric pyranosides and furanosides.
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The beta to alpha anomeric ratios of the blocked nucleoside is shown below.
Properly activated derivatives thereof in the anomeric center may have to be used.
The presence of a single anomeric signal connotes the presence of monosaccharide as a major component.
These enzymes are xylanases that hydrolyze with inversion of the anomeric configuration.
A nonreducing disaccharide has both anomeric carbons tied up in the glycosidic bond.
The nicotinamide moiety can be attached in two orientations to this anomeric carbon atom.
Nor does it include positions occupied by an anomeric hydroxyl group on a terminal monosaccharide unit.
As appears from the above formula the compound has two anomeric forms.
A new migration process of the anomeric group is included in the synthesis as a key step.
The anomeric carbon of the sugar binds to a free hydroxyl group on the lipid backbone.
Isomers that differ only in the configuration at the anomeric carbon are called anomers.
This anomeric mixture is then separated by fractional crystallization into the two configurational isomers.
Hyperconjugation can be used to explain phenomena such as the gauche effect and anomeric effect.
The enzymatic reaction induces cleavage of the anomeric bond and liberates the fluorophore group.
Each ring closure can have either an alpha or beta configuration at the anomeric position.
Any undissolved anomeric mixture will dissolve after the acid is added to the isopropanol solution.
These parts are bonded to each other via the anomeric carbon atom of the sugar.
Anomeric mixtures are expressed as a weight / weight ratio.
The choice of solvent mixture had a significant influence on the anomeric selectivity and conversion.
Anomeric mixtures are expressed as a weight / weight ratio or as a percent.
Our last results obtained from reductions of the anomeric tosylale group were the most promising.
The spectrum obtained showed the presence of four distinct saccharide components in the anomeric region.
The enzymatic reaction induces a cleavage of the anomeric bond and releases the fluorophore group.
The compound of formula I is normally obtained as a mixture of both anomeric forms.
Both the pure a and B anomers and the anomeric mixture are suitable for subsequent transformations.
This is very favourable because analytical data shows that the coupling anomeric selectivity is low.
For residue b and c, the anomeric resonances partially overlapped.
Said amino sugars can exist in a and B anomeric forms.
The anomeric alcohol was liberated, and the trisaccharide was coupled to ceramide 5.
Said aminosugars may exist in anomeric forms a or B.
The initial anomeric ratio of products is dependent on the initial anomeric composition of compound 2.
The invention includes both the mixtures and the separate anomeric forms a and B.
The maltose released has the beta anomeric configuration, hence the name beta-amylase.
Synthetic pathway of di-saccharide with an a anomeric linkage.
The anomeric configuration in these C-glycosides was determined by a chemical correlation.
