The amidine rearrangement in 5-amino-6-aryl-1,2,4-triazine-4-oxides initiated by hydroxylamine
β Scribed by Oleg N Chupakhin; Valery N Kozhevnikov; Anton M Prokhorov; Dmitry N Kozhevnikov; Vladimir L Rusinov
- Book ID
- 104210807
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 97 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
In this study 2-amino-4,6-didodecylamino-1,3,5-triazine (ADDT) was synthesized from cyanuric chloride and covalently functionalized onto graphene oxide nanosheets. The chemical structure of the alkylated melamine and the functionalized graphene oxide (GO) nanosheets were characterized with 1 H NMR,
The thermal rearrangement of 2,4-di(N-aryl)amino-1,3,5-triazin-6yl-prop-2-ynyl ethers 6-methyleneimidazo(l,2-a)-1,3,5-triar + yield a mixture of ne4-one & and 6-methylimidazo(l,2-a)-1,3,5-triazine-4-one 1, whereas under the influence of mercuric trifluroacetate the ethers 3 yield only 9. at room tem