Effect of N-alkylation on the position of conformational equilibrium in cis-decahydroquinoline
Abstract
1 H, 13C, and 19F Magnetic resonance studies of N-substituted cis-decahydroquinolines show that the type (2) conformation is preferred for substituents H and CH3, but that type (1) is preferred for CD2CH3 and CD2CF3.