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- W2055680165 abstract "In the presence of a catalytic amount of NaOH, the selective N-alkylation of various heteroaromatic primary amines is reported. With 1 equiv of NaOH, N1,C5-dialkylation of 4-phenyl-2-aminothiazoles has been investigated. Reaction of in situ generated aldehyde with amine yields the N-alkylated and N1,C5-dialkylated products through hydride ion transformation from alcohol." @default.
- W2055680165 created "2016-06-24" @default.
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- W2055680165 date "2013-06-24" @default.
- W2055680165 modified "2023-10-07" @default.
- W2055680165 title "Sodium Hydroxide Catalyzed <i>N</i>-Alkylation of (Hetero) Aromatic Primary Amines and N<sub>1</sub>,C<sub>5</sub>-Dialkylation of 4-Phenyl-2-aminothiazoles with Benzyl Alcohols" @default.
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- W2055680165 doi "https://doi.org/10.1021/jo400834h" @default.
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