Examples of 'intermediate can' in a sentence
Meaning of "intermediate can"
intermediate can - This phrase could refer to a container, such as a can, that contains or holds something of medium or moderate quality, size, or level. It suggests that the contents inside the can are not extremely basic or advanced, but rather fall in between
How to use "intermediate can" in a sentence
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intermediate can
This triprotected intermediate can be obtained in various ways.
Bituminous roofing, after cleaning and drying of the surface, Polyroof Intermediate can be applied.
This versatile intermediate can undergo several transformations.
Through such Y-glutamylation, Y-aminobutyraldehyde which is an aldehyde intermediate can be stabilized.
The cleaved peptide intermediate can then be isolated.
This intermediate can be coupled with a variety of reagents and compounds.
This method is efficient as each intermediate can be crystallized.
The polyether intermediate can be either a homopolymer or a copolymer.
Subsequent transformation of this intermediate can follow several paths.
This intermediate can then be reacted with an aldobionolactone.
Directing a synthesis toward a desirable intermediate can greatly narrow the focus of an analysis.
This intermediate can then be hydrolyzed with mild acid.
Or an amine-terminated tethered intermediate can be activated to an isocyanate.
The intermediate can be freeze dried or used in the next stage.
As a result, a reducing intermediate can no longer be produced.
See also
This intermediate can be carried on to the final product according to a variety of paths.
Naturally isolation of this intermediate can be effected, if so desired.
The intermediate can also be purified by several techniques known in the art.
Following workup, the desired intermediate can be isolated by crystallization.
The intermediate can then reduced to the oxidation state corresponding to anthralin.
Modification of the cycloaddition intermediate can lead to imides, lactams, and related compounds.
This intermediate can then be cyclized to a triazolone under refluxing aqueous potassium carbonate.
Unmasking is then a two stage process, but the intermediate can be subject to a purification step.
The imine intermediate can also be oxidized using quinone derivatives.
Additional Reference Examples, A useful intermediate can be prepared as follows,.
The desired intermediate can then be isolated and purified by conventional procedures.
Preferably, this is accomplished by transferring the intermediate can end 10 to a second forming station 33.
This intermediate can then be hydrolyzed to the final product as outlined below.
If desired, the 4-substituted piperidinyl intermediate can be purified by techniques known in the art.
The intermediate can cyclize and aromatize to provide the desired oxazole analog.
Formation of the anhydride intermediate can be inhibited by the presence of water.
A cyclized intermediate can undergo various types of modifications to generate the final natural product.
Alternatively, a similar intermediate can be formed using carbonyldiimidazole.
The intermediate can then be hydrolyzed to the acid III.
Synthesis of the key intermediate can be achieved according to Scheme VIII.
This intermediate can be prepared in a variety of ways from hydrazines I.
The resulting amide intermediate can be isolated by removal of the solvent.
This intermediate can be used to prepare benzoxazinones as outlined in Schemes I and II.
Accordingly, the polyether intermediate can be either a homopolymer or a copolymer.
This intermediate can be isolated, but is typically not.
The resulting nor-amine oxazole intermediate can be carried on to prepare various exemplified compounds.
This intermediate can then be nitrated, for example, to form polynitro intermediate.
Furthermore, such key intermediate can be prepared in both high yield and purity.
This intermediate can be coupled using a peptide coupling reagent to furnish spirocyclic hydantoin 19.
Furthermore, the said intermediate can be converted to pioglitazone at a good yield.
The intermediate can methylate nucleophiles, such as water and other biomolecules as shown below.
The resulting condensation intermediate can be further reduced to an amine ( -NH2 ).
This intermediate can then rearrange to form a Y-shaped adduct, which can undergo faster reductive elimination.
Incidentally, the reaction intermediate can be easily removed by using the above crystallizing method.
This intermediate can be made as shown in Scheme 1 which is illustrated following the examples.
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