The application of the 2-amino-4-pyrimidones to supramolecular synthesis

Nichtkovalente Synthese mit Wasserstoffbrücken

“…B. Homodimere auf der Basis von Carbonsäuren, [51,70] cis-und trans-Amiden, [71±75] Imiden, [76,77] Harnstoffen, [70,78] Oxalamiden [79] und 10-Hydroxy-10,9-borazarophenanthren [80] oder Heterodimere basierend auf Carbonsäuren und Amiden, [81] 2-Amido-sowie Aminopyridinen, [82,83] 2-Amino-4-pyrimidonen [84] oder Dipyrrinonen. Viele dimere Festkörperaggregate sind beschrieben worden, z.…”

Designing a Cocrystal of γ‐Amino Butyric Acid

“…Candidates for cocrystal formation with a particular structural motif for achieving desired physical properties5, 6 are chosen on the basis of their ability to utilize known intermolecular interactions in forming those crystals. Because hydrogen bonds are among the strongest and most preferentially directional intermolecular interactions, they have been the leading candidates for the interactions to be utilized in forming cocrystals,7–10 although other interactions have also been suggested 11a,b…”

Tautomeric Self‐Dimerization and Molecular Recognition Properties of2‐Aminopyrimidinone Derivatives as Triple Hydrogen‐Bonding Modules in Molecular Assemblies

“…They form complementary triple hydrogenbonding in an exact 1:1 ratio, which consists of two kinds of its tautomers perhaps in an ADD·DAA mode as seen in the literature. [6,8,9] Nucleobase Recognition Abilities of N-Alkyl-2-amino-3H-pyrimidin-4-one Derivatives 7 and 9…”