Examples of 'reduction of the nitro group' in a sentence
Meaning of "reduction of the nitro group"
reduction of the nitro group - This phrase describes a chemical reaction or process where a nitro group in a compound is converted to a different functional group through a reduction reaction
How to use "reduction of the nitro group" in a sentence
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reduction of the nitro group
The reduction is a reduction of the nitro group.
Reduction of the nitro group can provide anilines.
Nitration followed by reduction of the nitro group yields the aniline.
Reduction of the nitro group gives a biaryl amine derivative.
Nitration of an aromatic precursor followed by reduction of the nitro group yields the aniline.
Reduction of the nitro group may be achieved in a conventional manner.
Step 2 is a reduction of the nitro group.
Reduction of the nitro group may be achieved by conventional means.
Compound E1 can be obtained from compound D1 via reduction of the nitro group.
The reduction of the nitro group gave the title compound.
Step 6 is analogous to Reference Example 166, describing a Raney nickel reduction of the nitro group.
The reduction of the nitro group gives the title compound.
We then carried the reduction of the nitro group present in the synthesized quinolines.
Reduction of the nitro group can be achieved using methods known in the art.
Stage 2A involves the reduction of the nitro group of Compound B to the corresponding aniline ( 4 ).
See also
Reduction of the nitro group in XIII is achieved using standard procedures known in art.
Subsequent reduction of the nitro group using the methods described above yields compounds of structure 2.
Reduction of the Nitro group.
Selective reduction of the nitro group to the corresponding amine with tin ( II ) chloride provides 7e.
Reduction of the nitro group of XIV gives the amino compound XV.
Finally, reduction of the nitro group provides 34.
The reduction of the nitro group can be carried out by conventional means.
Reduction of the nitro group was accomplished using hydrogen and Raney nickel in THF.
Upon reduction of the nitro group by a nitroreductase, the dye becomes fluorescent.
Reduction of the nitro group followed by alkylation of the resulting aniline then gives 16.
Reduction of the nitro group can be carried out with a variety of well-known reducing agents.
Reduction of the nitro group affords the aniline of Formula 4.
Reduction of the nitro group and the amide is then analogous to Method IX . i.
Reduction of the nitro group and sulfonation of A-3a was carried out under standard conditions.
Reduction of the nitro group followed by addition of formamidine acetate provides the benzimidazole I ( G ).
Reduction of the nitro group gives the aniline 18.
Reduction of the nitro group of 8e provides the desired amino-indole 8f.
Reduction of the nitro group and cyclization to the lactam are effected as in ( 1 ).
Reduction of the nitro group finally gives the desired anilines of formula ( 2 ).
Reduction of the nitro group to yield ( 2g ) is accomplished under standard reaction conditions.
Reduction of the nitro group with SnCl 2 yielded the aniline derivatives 2.
Reduction of the nitro group in the intermediates 8a and 8b afforded the corresponding amino derivatives 9a and 9b.
Reduction of the nitro group with tin ( II ) chloride is followed by spontaneous cyclization to enamine F-2.
Reduction of the nitro group yields intermediate ( XI-a ).
Reduction of the nitro group in 14 provides an amine of formula 15.
Reduction of the nitro group in 19 then provides intermediate 20.
Reduction of the nitro group of 7b provides the amino-indole 7c.
Reduction of the nitro group to amino following preceding methods affords ( 28 ).
Reduction of the nitro group in arylpropionic acid ( 1 ) gives the corresponding aniline ( 2 ).
Reduction of the nitro group ( for example using catalytic hydrogenation ) produces 2 ( iii ).
Reduction of the nitro group in intermediates 5a and 5b gives the 6-aminopyridine derivatives 6a and 6b.
Reduction of the nitro group in intermediates 5a and 5b gives the 4-aminobenzoyl derivatives 6a and 6b.
Reduction of the nitro group in intermediate 5 gives the 4-aminobenzoyl derivative 6a and the 6-aminonicotinoyl derivative 6b.
Reduction of the nitro group followed by condensation with 3-ethoxy-3-iminopropionic acid ethyl ester gave 6.
Reduction of the nitro group in 15 as described in Scheme 1 provides compounds of formula 16.
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