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- W2949939863 abstract "Treatment of 3-substituted 7-amino-5-hydroxy-primido[5,4-e]-as-triazine 4-oxides (IIIa—d) with acetic anhydride or alcoholic sodium hydroxide caused a benzylic acid-type rearrangement followed by decarboxylation and dehydration to give the corresponding 6-acetylaminoimidazo[4,5-e]-as-triazines (IVa—d) or 3-aminoimidazo[4,5-e]-as-triazines (Va—c); similarly, 3-substituted toxoflavin 4-oxides (VIa—c) gave the respective 1,5-dimethyl-1H-imidazo[4,5-e]-as-triazin-6-(5H)-ones (VIIa—c), and 3-substituted fervenulin 4-oxides (VIIIa—c) gave the respective 5,7-dimethyl-5H-imidazo[4,5-e]-as-triazin-6(7H)- ones (IXa—c)." @default.
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- W2949939863 date "1976-12-07" @default.
- W2949939863 modified "2023-09-24" @default.
- W2949939863 title "ChemInform Abstract: 6-AZAPURINES (IMIDAZO(4,5-E)-AS-TRIAZINES)" @default.
- W2949939863 cites W2002410404 @default.
- W2949939863 doi "https://doi.org/10.1002/chin.197649228" @default.
- W2949939863 hasPublicationYear "1976" @default.
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