Kafka, Zdenek published the artcileNitrogeneous compounds of adamantane. XI. Paper chromatography and thin-layer chromatography of some derivatives of 1,3,5-triazaadamantane, Application In Synthesis of 14707-75-6, the publication is Sbornik Vysoke Skoly Chemicko-Technologicke v Praze, D: Technologie Paliv (1977), 119-26, database is CAplus.
1,3,5-Triazaadamantane (I), nitro and amino derivatives of I, and their quaternary salts were separated by paper chramatog. (Whatman number 1, 20¡ã, descending) and thin-layer chromatog. on silica gel and Al2O3 (ascending). RF values are given for I, 7-nitro-1,3,5-triazabicyclononane (II), II N-oxide, 3,7-diacetyl-5-nitro-1,3,7-triazaadamantane (III), III N-oxide, 7-amino-1,3,5-triazaadamantane (IV), IV nicotinate, IV isonicotinate, IV adipate, IV glutarate, 7-nitro-1,3-diaza-5-methylazoniaadamantane iodide, 7-nitro-1,3-diaza-5-ethylazoniaadamantane iodide, 7-amino-1,3-diaza-5-methylazoniaadamantane iodide, 7-amino-1,3-diaza-5-ethylazoniaadamantane iodide, and N,N’-bis(1,3,5-triaza-7-adamantyl) urea for 13 binary and ternary solvent systems used in paper chromatog. The quaternary salts and bicyclononane derivatives were separated with HCl or AcOH containing systems.
Sbornik Vysoke Skoly Chemicko-Technologicke v Praze, D: Technologie Paliv published new progress about 14707-75-6. 14707-75-6 belongs to catalysis-chemistry, auxiliary class Triazinanes, name is 1,3,5-Triazaadamantan-7-amine, and the molecular formula is C7H14N4, Application In Synthesis of 14707-75-6.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia