The biobased renewable monomer 2,5-diformylfuran is polymerised using various N-heterocyclic carbene (NHC) catalysts in dimethyl sulfoxide (DMSO) affording a low molar mass polymer. It shown that catalyst structure as well the temperature and time polymerization running have noticeable effect on its mass. obtained material characterized by nuclear magnetic resonance (NMR), thermogravimetric ana...

New mechanochemical pathways for the transformation of six N-heterocyclic carbonyl compounds into oximes using hydroxylamine hydrochloride were explored. Reactions were performed first without any base since the heterocyclic moieties (imidazole, benzimidazole, pyridine and quinuclidine) have an intrinsic basic nitrogen atom. This green, solvent free method was suitable for all compounds (up to ...

In the title mol-ecule, C(16)H(20)N(2)OS, the heterocyclic ring adopts a slightly distorted flattened boat conformation, and the plane through the four coplanar atoms makes a dihedral angle of 86.98 (6)° with the benzene ring. The thione, acetyl and methyl groups lie on the opposite side of the heterocyclic mean plane to the isopropylphenyl group which has an axial orientation. A weak intra-mol...

The asymmetric unit of the title N-heterocyclic carbene compound, C(22)H(32)N(4) (2+)·2PF(6) (-), consists of one half of the N-heterocyclic carbene dication and one hexa-fluoro-phosphate anion. The dication lies across a crystallographic inversion center. The imidazole ring is twisted away from the central benzene ring, making a dihedral angle of 76.23 (6)°. The hexa-fluoro-phosphate anions li...

The complete molecule of the title compound, C(31)H(42)N(2)O(6), is generated by crystallographic twofold symmetry, with one C atom lying on the axis. The dihedral angle between the aromatic rings is 57.03 (6)°. The central heterocyclic ring adopts a half-chair conformation. The mol-ecular conformation is stabilized by two intra-molecular O-H⋯N hydrogen bonds with the N atoms of the heterocycli...

Heterocyclic sulfones and sulfonamides represent important structural motives in medicinal chemistry drug development. Therefore, efficient reliable methods for their construction from simple building blocks are high demand. Herein we report a novel approach the direct C–H-sulfonylation of N-heteroaromatics via N-activation with triflic anhydride (Tf2O), base-mediated addition sulfinate salt su...