Examples of 'corresponding amine' in a sentence
Meaning of "corresponding amine"
corresponding amine: This phrase typically relates to chemistry and organic compounds, where an amine is a derivative of ammonia. The term 'corresponding' implies a relationship or connection between different substances or molecules
How to use "corresponding amine" in a sentence
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corresponding amine
The corresponding amine was isolated in tetrahydrochloride form.
A halo may be converted to the corresponding amine.
The corresponding amine was isolated in dihydrochloride form.
The azide is catalytically reduced to the corresponding amine.
The corresponding amine was obtained by liberating the hydrochloride.
Each diastereomer was reduced separately to give the corresponding amine.
The final HCl salt of the corresponding amine was typically used without further purification.
The second step comprises reductive alkylation of the corresponding amine.
Subsequent reaction is with the corresponding amine components under the conditions of a nucleophilic substitution reaction.
Hydrolysis and decarboxylation of the isocyanate then yields the corresponding amine.
Intermediate O was then reduced to the corresponding amine P under standard conditions.
The resulting adduct is treated with aqueous acid to provide the corresponding amine.
The corresponding amine is added and the mixture is stirred at RT for 3 days.
Imines are susceptible to hydrolysis to the corresponding amine and carbonyl compound.
The resulting mixture was stirred until complete conversion of imine intermediate to the corresponding amine.
See also
The reduction of the hydroxyimino allows the corresponding amine compound to be obtained.
Chlorination of compound ( 6 ) with thionyl chloride, followed by azidation and reduction affords the corresponding amine.
The nitro substituent can be reduced to the corresponding amine 8a under standard conditions.
The remaining ammonium cation salts showed solubility effects related to the corresponding amine.
Thereafter, a reductive reaction with the corresponding amine is carried out to obtain a compound ( 5 ).
The amine functionality is at least partially neutralized to produce the corresponding amine salt.
Or to the corresponding amine compound of formula ( VIII ),.
The resulting solid was filtered to provide the corresponding amine hydrochloride salt.
Of the corresponding amine and the tube heated to 130°C and the reaction followed by LC / MS.
Cleavage of the Teoc protecting group with acid affords the corresponding amine compounds.
Selective reduction of the nitro group to the corresponding amine with tin ( II ) chloride provides 7e.
The ester is then saponified ( ) and the nitro group reduced to the corresponding amine.
Conversion of 20 to 21 is accomplished with the corresponding amine in the presence of base . a.
Separating the avidin-containing substrate and reducing the formed imino bond to the corresponding amine bond ;.
Ii where T is - CN, by reduction to its corresponding amine of formula -CH2NH2.
The deprotection of the compound of formula ( I ) gives rise to the corresponding amine.
Reduction of the azide of formula XIV yields the corresponding amine of formula XV.
Scheme 3 describes a preparation of the key isocyanate intermediate 4 from the corresponding amine 1.
In a first step, the nitrile is reduced to the corresponding amine IIIc.
Scheme 2 describes a preparation of carbamates and mono - N - akyl ureas from the corresponding amine 1.
Reducing the imine of the formula, to produce the corresponding amine of the formula,.
Alternatively, other well-known methods for converting a nitro-group to its corresponding amine may be used.
Processes for hydrogenating an aromatic nitro compound, thereby providing a corresponding amine are well known.
Step ( xix ) comprises reaction with the corresponding amine.
This is suitably achieved by converting such a compound to the corresponding amine ( XX ) 1.
The Z-group is removed vía standard hydrogenation conditions to yield the corresponding amine ( Formula 8 ).
Cyano derivative 86 can be then reduced to the corresponding amine 85.
Y2=Y1 but preferred reactivity through steric control with the corresponding amine 6.
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