Examples of 'n-oxides' in a sentence
Meaning of "n-oxides"
N-oxides (noun) - Chemical compounds that contain one or more nitrogen atoms bonded to an oxygen atom
How to use "n-oxides" in a sentence
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n-oxides
N-oxides of the ring nitrogens are also included.
Preferred chelants include anionic catechols, particularly catechol sulphonates, hydroxamates and hydroxypyridine N-Oxides.
N-oxides of the compounds mentioned above belong to the invention.
Examples of the structures of such N-oxides are as follows.
N-oxides of tertiary nitrogen atoms are also included in the invention.
Tertiary amines cleanly give the corresponding N-oxides.
N-oxides may be rearranged in trifluoroacetic acid to give the hydroxypyridines.
Process for converting tertiary amine N-oxides to aldehydes.
N-oxides of the pyridyl nitrogen can be prepared using standard techniques.
The nitrogen atoms may be in the form of N-oxides.
N-oxides can be formed following procedures known to the skilled person.
And their salts or solvates and their N-oxides.
N-oxides of the ring nitrogens for all heteroaryl groups are also included.
The nitrogen atoms can be in the form of N-oxides.
N-oxides may be formed conventionally by reaction with hydrogen peroxide or percarboxylic acids.
See also
The compounds of the invention also include N-oxides.
N-oxides of the compounds mentioned above are in the scope of the present invention.
Or pharmaceutically acceptable salts or N-oxides thereof.
N-oxides of the compounds are the compounds where nitrogen of the compounds is oxidized.
Or an agrochemically acceptable salt or N-oxides thereof.
N-oxides are oxidized forms of tertiary amines or oxidized forms of nitrogen containing heteroaromatic compounds.
And pharmaceutically acceptable salts and N-oxides thereof.
N-oxides are oxidised forms of tertiary amines or oxidised forms of nitrogen containing heteroaromatic compounds.
The term heteroaryl is meant to include possible N-oxides.
N-oxides may be more active than their corresponding tertiary amines or less active.
The present invention includes all such possible N-oxides.
N-Oxides are also contemplated to be included in the present invention.
The present disclosure includes all such possible N-oxides.
Pyridine N-oxides can be obtained by oxidation of the corresponding pyridines.
Hydrates of such compounds and their N-oxides and prodrugs.
Different N-oxides can be separated by conventional methods such as chromatography.
Compounds containing an amine function may also form N-oxides.
The polyamine N-oxides can be obtained in almost any degree of polymerization.
Nitrogen heterocycles can also be present as N-oxides or as quaternary salts.
The polyamine N-oxides can be obtained in almost any degree of polymerisation.
Ring nitrogen atoms may be optionally oxidized to form N-oxides.
And the N-oxides and the agriculturally acceptable salts thereof.
Ring nitrogen atoms maybe optionally oxidized to form N-oxides.
Heteroaryl N-oxides can be produced by methods known to the skilled person.
The invention extends to all such salts and N-oxides.
The optionally substituents include N-oxides of the ring nitrogen atoms.
Nitrogen containing heterocyclyl and heteroaryl residues may form N-oxides.
These data support screening the use of N-oxides in an enhancement solution.
Tertiary amine N-oxides are hereinafter on occasion referred to for convenience as amine oxides.
Examples of pharmaceutically acceptable salts also include internal salts such as N-oxides.
Recently, the use of amine N-oxides has been reported to produce aldehydes directly.
Or a pharmaceutically acceptable salt, a solvate or hydrate thereof or one or more N-oxides thereof.
In general, reduction of picolinate N-oxides can be used to prepare the corresponding picolinates.
In a general manner, nitrogen heterocycles can also be present as N-oxides or as quaternary salts.
Also envisioned art N-oxides of the compounds in cases where such can be prepared.
