Examples of 'can be alkylated' in a sentence
Meaning of "can be alkylated"
can be alkylated: In chemistry, the term 'can be alkylated' refers to a compound or molecule that is able to undergo alkylation, a specific type of reaction where an alkyl group is transferred to another molecule
How to use "can be alkylated" in a sentence
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can be alkylated
The amino group can be alkylated if desired.
The resulting sodium derivatives can be alkylated.
Free hydroxyl groups can be alkylated in an analogous manner.
Phenolic groups on the monomer can be alkylated.
Benzene can be alkylated with benzylchloride to form diphenylmethane.
The resulting amino compounds in turn can be alkylated or acylated.
The amino group can be alkylated by reductive amination procedures.
In particular the nitrogen atom of the pyrrole nucleus can be alkylated.
Corresponding alcohols can be alkylated or acylated using standard procedures.
Both molecules have a cyclic tertiary alkyl amine group at one terminus that can be alkylated.
Many aromatic hydrocarbons can be alkylated using the present invention.
If desired, the amino group of the benzamide compound obtained can be alkylated.
The imine can be alkylated and also serves as a ligand in coordination chemistry.
By alkylatable is meant that the aromatic compound can be alkylated by an olefinic compound.
Amide 3 can be alkylated with methyl acrylate to give a tertiary amide.
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In both cases the amide or amino nitrogens can be alkylated by lower alkyl groups.
The amine can be alkylated with an alkyl, heteroalkyl or haloalkyl substituted with a leaving group.
Alternatively, the nitrogen atom can be alkylated.
The pyrazole intermediates can be alkylated using the general procedure described below.
Likewise, phosphonate-stabilized carbanions can be alkylated.
Phenolic groups on the monomer can be alkylated to produce polar and nonpolar substituents.
Thioanisole undergoes deprotonation with alkyllithium reagents to afford C6H5SCH2Li, which can be alkylated.
If desired, the amino group can be alkylated by a well known method.
Hg ( II ) can be alkylated by treatment with diazonium salts in the presence of copper metal.
It is known that aromatic hydrocarbons can be alkylated in the presence of acid-treated zeolite.
Indole 1 can be alkylated with a halide at the 3-position to give 2 under basic conditions.
Alkylphenols such as decyl, nonyl, octyl or other phenols can be alkylated using polyalkylenes.
Additionally, phenols can be alkylated by a variety of common methods to prepare ethers.
To study Brazzein conformation, the protein 's cysteines can be alkylated.
Mercaptan intermediate 12 can be alkylated or acylated with typical electrophiles to produce new analogs.
Alternatively the product from step 1 ( Intermediate A ) can be alkylated e . g.
Aromatic hydrocarbons which can be alkylated are both monocyclic and polycyclic, also alkylsubstituted.
Ring nitrogens such as the N1 of adenine, N7 of guanine, N3 of cytosine can be alkylated.
Groups that can be alkylated in this way include thiols, alcohols, imines and carboxylic acids.
Finally, the resulting isoquinolone g102 can be alkylated as described in Scheme 1.
The latter can be alkylated with the sodium salt of 2-chloroacetic acid.
The R1 of the resulting Compound ( 1a ) can be alkylated or aralkylated as desired.
In turn, this can be alkylated with benzyl bromide under similar conditions to yield g26.
Alternatively in step A, the tetra N-tosylated amine ( 23 ) can be alkylated under Mitsunobu conditions.
The thionocarbamates can be alkylated as illustrated in Step 2 using known methods R.
C1 can be alkylated with e.g. propargyl bromide towards compound C2.
Compounds where R2 is hydrogen can be alkylated and acylated by standard methods.
They can be alkylated on oxygen and used as a dipole in 1,3-dipolar cycloadditions.
Compounds of Formula 42 can be alkylated with a variety of bases.
Such compounds can be alkylated by conventional procedures to form those wherein R ⁹ = ( halo ) alkyl.
Method E Dimethyl malonate can be alkylated with bromide 17 and a base.
This phenol can be alkylated using an electrophile ( YX ) to provide the alkylated product ( I-8 ).
If desired, sulfonamide intermediate 5 can be alkylated at the sulfonamide nitrogen atom to provide compound 6.
The intermediate ( IIb ) can be alkylated as described above to produce a compound of formula ( III ).
The N, O-bis-BOC-hydroxylamine can be alkylated in the following manner.
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Thiols are readily alkylated to give thioethers
The alkylated liquid produced is analyzed by gaschromatography
At least one conventional alkylated diphenylamine antioxidant
