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Nucleophilic aromatic substitution of methyl 3‐nitropyridine‐4‐carboxylate

18

Citations

4

References

2004

Year

Abstract

Abstract The nitro group of methyl 3‐nitropyridine‐4‐carboxylate ( 1 ) has successfully been replaced by nitrogen, oxygen and sulphur nucleophiles by nucleophilic aromatic substitution to give the 3‐azido, 3‐methoxy, 3‐phenoxy and 3‐thiophenoxypyridine‐4‐carboxylates ( 2a — d ).

References

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