Asymmetrische reduktive Aminierung von Cycloalkanonen 8. Mitt. Die EPC‐Synthese arylsubstituierter cis‐4aR, 10bR‐ und cis‐4aS, 10bS‐Octahydrophenanthridine
- 1 January 1989
- journal article
- research article
- Published by Wiley in Archiv der Pharmazie
- Vol. 322 (4) , 199-206
- https://doi.org/10.1002/ardp.19893220403
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Asymmetrische reduktive Aminierung von Cycloalkanonen, 7. Mitt. Die asymmetrische Synthese von cis‐1R,2R‐ und cis‐1S,2S‐2‐ArylcyclohexanaminenArchiv der Pharmazie, 1989
- Synthesis of cis- and trans-1-(3,4-dimethoxybenzyl)-3,7-dimethyl-5,8-dimethoxy-1,2,3,4-tetrahydroxyisoquinoline. Mechanism of the Bischler-Napieralski reactionThe Journal of Organic Chemistry, 1974
- 7,8,9-Trimethoxy-4a,10b-trans- and -4a,10b-cis-1,2,3,4,4a,5,6,10b-octahydrophenanthridines. Configurational and conformational changes in epimerization of N-substituted derivativesThe Journal of Organic Chemistry, 1972