The naphthol-containing mol-ecule of the title compound, C10H6Br2O·CH3OH, crystallized as a methanol monosolvate and is planar to within 0.069 (1) Å for all non-H atoms. In the crystal, mol-ecules are linked by two pairs of O-H⋯O hydrogen bonds, involving the methanol mol-ecule, forming dimer-like arrangements. The crystal structure is further stabilized by π-π stacking [centroid-centroid dista...

The application of the Nicholas reaction chemistry of 2,7-dioxygenated naphthalenes in the synthesis of cyclohepta[de]napthalenes and in the synthesis of (±)-microstegiol (1) is presented. The substitution profile of Nicholas monosubstitution (predominantly C-1) and disubstitution reactions (predominantly 1,6-) on 2,7-dioxygenated napthalenes is reported. Application of a 1,8-dicondensation pro...

This paper reports the synthesis of 14 diazophthalocyanins containing Mg, Cu, or Pb as the chelated metal. To assess the usefulness of these compounds for fine structural cytochemistry, the relative coupling rates with naphthols were tested as well as the solubility of the resulting azo dyes. Three of the diazotates were reacted with tissue proteins in aldehyde-fixed material, and the density i...

A facile and eminent method has been reported for the preparation of amido alkyl naphthols. Amido naphthol derivatives were synthesized by condensation pyrazole aldehydes, β-naphthol acetamide in presence a heterogeneous SiO2 supported sodium hydrogen sulphate catalyst using acetic acid as solvent. This protocol is advantageous its shorter reaction hours, simplest workup technique, excellent yi...

An efficient and environmentally benign one-pot condensation of cyclic diketones, aldehydes naphthols was achieved with 1,4-diazabicyclo[2-2-2]octane supported on Amberlyst-15 as a novel catalyst, producing variety benzoxanthenones in good to excellent yields. The advantages this multicomponent reaction include the use heterogeneous solventless conditions simple methodology that is atom-economi...