The stereoselective synthesis of 2,6-dimethyl-1,5-diaza-cis-decalins with the dimethyl groups syn or anti to the angular hydrogens has been accomplished starting from 1,5-diaza-cis-decalin. From an NMR study of the conformational properties of all three 2,6-dimethyl-1,5-diaza-cis-decalins, the components which affect the conformational equilibrium have been identified. © 2001 Elsevier Science Ltd.
Kozlowski, M. C., Xu, Z., & Santos, A. G. (2001). Synthesis and conformational analysis of 2,6-dimethyl-1,5-diaza-cis-decalins. Tetrahedron, 57(21), 4537–4542. https://doi.org/10.1016/S0040-4020(01)00370-2