REVUE ROUMAINE DE CHIMIE, cilt.36, sa.8, ss.925-929, 1991 (SCI-Expanded)
1-Naphthylcycloalkanols having 3, 4, 5, 6, 7, 12 and 15 ring carbons were synthesized from corresponding cyclic ketones and 1-naphthylbromide using Grignard reaction. The dehydration products of these naphthylcycloalkanolis were obtained. All the products were identified by means of IR- and H-1-NMR spectra.