Burkhard, Jiri published the artcileReactivity of triformylmethane. Part II. Reactions of triformylmethane with adamantane derivatives containing primary amino group, Safety of 1,3,5-Triazaadamantan-7-amine, the publication is Collection of Czechoslovak Chemical Communications (1992), 57(9), 1947-50, database is CAplus.
Six new compounds, e.g., RNHCH:C(CHO)2 (R = R1, R1CO, R1NHCO; R1 = 1-adamantyl) were obtained by condensation of triformylmethane with some aminoadamantane derivatives RNH2. The study also includes the reaction of 7-amino-1,3,5-triazaadamantane I (R = H) with triformylmethane to give I [R = CH:C(CHO)2]. S-1-Adamantyl)isothiourea hydrochloride reacted with triformylmethane to give pyrimidine derivative II (R = 1-adamantyl).
Collection of Czechoslovak Chemical Communications 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, Safety of 1,3,5-Triazaadamantan-7-amine.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia