Conformational studies on 2-methyl- and 2,NN-trimethyl-chroman-3-amine and derivatives

Abstract
The synthesis of cis- and trans-2-methyl- and 2,NN-trimethylchroman-3-amines is described. Configurations and preferred conformations are assigned to the free bases, and to derivatives (hydrochlorides, N-acetyl, N-phthaloyl) by interpretation of proton magnetic resonance spectra recorded at 220 MHz.