Constraining a peptide in its bioactive conformation by macrocyclization represents a powerful strategy to design modulators of challenging biomolecular targets. This holds particularly true for the development of inhibitors of protein-protein interactions which often involve interfaces lacking defined binding pockets. Such flat surfaces are demanding targets for traditional small molecules ren...

The macrocyclic nonaaza 3 + 3 amine based on diaminocyclopentane forms enantiopure helical complexes with lanthanide(III) ions. In contrast to analogous complexes based on 1,2-trans-diaminocyclohexane, no clear helicity process is observed. Crystal structures of these compounds show tight helical wrapping of the macrocycle around the lanthanide(III) ion leading to the formation of a double heli...

The triphosphorus macrocycle 1,5,9-triethyl-1,5,9-triphosphacyclododecane, 12[ane]P3Et3, reacts with [V(CO)6] under photolytic conditions to produce fac-[(12[ane]P3Et3)V(CO)3] (1) which has been isolated as its Et4N salt. This can be oxidised to the neutral 17 electron complex fac-(12[ane]P3Et3)V(CO)3 (2), which has been characterised by EPR spectroscopy. Density functional calculations support...

Chiral hexaazamacrocycles with a trianglamine structure and C(3)-symmetry, containing six ring substituents and twelve stereocenters have been tested as chiral solvating agents (CSAs) for α-substituted carboxylic acids. Excellent results have been obtained with a hexaphenyl-substituted macrocycle. The optimal ratio between the macrocycle and racemic acid, allowing for baseline separation of the...

Facile synthesis and postsynthetic modification of a rectangular 1,2,4-triazole-based NHC macrocycle have been developed. The silver complex [Ag2(1)2](BF4)2 is derived from the corresponding triazole salt H2-1(BF4)2 upon reaction with Ag2O. The structure of the metallocyclic Ag-NHC complex [Ag2(1)2](BF4)2 was determined by single-crystal X-ray diffraction analysis. The metal-carbene template un...

In the title compound, C(24)H(44)N(6) (6+).6C(7)H(7)O(3)S(-).2H(2)O, the macrocycle crystallizes in its hexaprotonated form, accompanied by six p-toluenesulfonate ions and two water molecules, and lies on an inversion center. The three independent p-toluenesulfonate anions and their inversion equivalents at (1 - x, 1 - y, 1 - z) are linked to the macrocyclic cation through N-Hcdots, three dots,...

A simple macrocyclic amine is alkylated by methylene chloride to give a quaternary ammonium chloride salt. When methylene chloride is the solvent, the reaction exhibits pseudo-first-order kinetics, and the reaction half-life at 25.0 degrees C is 2.0 min. The reaction half-life for a structurally related, acyclic amine is approximately 50 000 times longer. Detailed calculations favor a mechanism...