Examples of 'anomers' in a sentence
Meaning of "anomers"
Anomers is a noun used in chemistry to describe stereoisomers that differ only in the configuration at the hemiacetal or hemiketal carbon atom
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- plural of anomer
How to use "anomers" in a sentence
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anomers
This structural difference distinguishes two anomers.
Anomers can be interconverted through a process known as mutarotation.
Attempts to separate the anomers by fractional crystallization were unsuccessful.
Anomers may be separated by conventional methods.
The resulting possible pair of stereoisomers is called anomers.
Either pure anomers or anomer mixtures may be used.
Further column chromatography gave more of the separated anomers.
The α and β anomers of glucose.
These nucleoside anomers are typically separated by a physical means such as crystallization or chromatography.
The reaction typically produces a mixture of ß and a anomers that must be separated.
Beta nucleoside anomers are useful and important as pharmacologically active compounds.
Isomers that differ only in the configuration at the anomeric carbon are called anomers.
The ratio of the two anomers is specific for the regarding sugar.
Processes for preparing nucleosides frequently result in a mixture of alpha and beta nucleoside anomers.
The alpha and beta anomers were separated by silica gel column chromatography.
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The silyl protected nucleosides could not be resolved by column chromatography into the separate anomers.
The fractions corresponding to each of the a and B anomers are combined and concentrated under vacuum.
A portion of this material was recrystallized from toluene affording a clean separation of the a and B anomers.
Both the pure a and B anomers and the anomeric mixture are suitable for subsequent transformations.
The reaction typically produces a mixture of B and a anomers that must be separated.
Both a and B anomers and mixtures thereof may be used.
The present invention includes the use of both individual a and B separate anomers and their mixtures.
The two anomers of the cyclic forms are represented by a and B.
They may exist in the form of a or B anomers.
The alpha / beta anomers were separated by silica gel column chromatography.
The characteristics of the a and B anomers are given below.
The two different forms of cyclic sugars, alpha and beta, are referred to as anomers.
However, we have found that the alpha anomers are more effective structurants.
The product was obtained as a mixture of the a and B anomers.
Because anomers are diastereomers of each other, they often differ in physical and chemical properties.
The disaccharides content remains constant, heating influencing only the methyl glucoside alpha / beta anomers ratio.
The a and B anomers thus obtained are characterized by the following analytical methods,.
The product of the glycosylation may be a single anomer ( a or B ) or a mixture of both anomers.
Confirms the esterification of the anomers a and B in position 2 of the desosamine ring.
The process of claim 8, wherein the reaction produces a mixture of a and B anomers.
This latter procedure also results in the B anomers of cellobiose, maltose and maltotriose.
The a and B anomers may be optionally separated, for example by chromatography on a silica column.
The material obtained after chromatography was the unresolved a / B anomers.
Preferred furanosylamines are the beta and alpha anomers of D and L ribose, xylose and arabinose.
The reaction was complete in 5 h to give a mixture of a - and B - anomers.
Note 1, The diastereomeric anomers do not separate.
FIG . 10D shows the specificity of lectin binding to different anomers.
Preferred furanosylamines are the beta and alpha amino anomers of D - and L-ribose, xylose and arabinose.
The filtrate contained a 1:1 ratio of the two anomers.
NMR clearly shows two ( a and B ) anomers in carbon NMR.
HPLC analysis showed an approximate 1:1 mixture of a and anomers.
Fig . 1 B, HPLC chromatogram of pure punicalagin anomers isolated from TPT.
After quenching the reaction in a weakly acidic aqueous solution, a mixture of 1, 1 anomers was obtained.
These effects are illustrated in the CP / MAS spectra of the? and? anomers of methyl-D-xylopyranoside.
The other containing a mixture of the a and B anomers ( 92 mg ).
