Asymmetrische α‐Amidoalkylierung: Synthesen enantiomerenreiner α‐substituierter Piperidine mit 1‐Camphanoyl‐1,2,3,4‐tetrahydropyridin
- 1 December 1987
- journal article
- research article
- Published by Wiley in Archiv der Pharmazie
- Vol. 320 (12) , 1253-1267
- https://doi.org/10.1002/ardp.198700043
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- Synthesis of optically active piperidine and pyrrolidine alkaloids from L-lysine, L-ornithine, or L-proline using anodic oxidation as key stepsThe Journal of Organic Chemistry, 1986
- α-Amidoalkylation at Carbon: Recent Advances - Part ISynthesis, 1984
- Stereoselective synthesis of brassinolide: a plant growth promoting steroidal lactoneJournal of the American Chemical Society, 1980
- Rapid chromatographic technique for preparative separations with moderate resolutionThe Journal of Organic Chemistry, 1978
- (2-Piperidine)- and (2-pyrrolidine)ethanones and -ethanols as inhibitors of blood platelets aggregationJournal of Medicinal Chemistry, 1976
- Further side-chain modification of antimalarial phenanthrene amino alcoholsJournal of Medicinal Chemistry, 1973
- Variation in toxicologic response of species to an analgesicToxicology and Applied Pharmacology, 1967
- Synthese und absolute Konfiguration von (+)‐8‐Phenyl‐norlobelol‐i [(+)‐Norallosedamin] aus Lobelia inflata LEuropean Journal of Organic Chemistry, 1959
- Synthese und absolute Konfiguration von (—)‐Sedamin und von (—)‐8‐Phenyl‐lobelol‐i [(—)‐Allosedamin]European Journal of Organic Chemistry, 1959
- Die Kondensation von Δ1‐Piperidein mit Acetessigsäure und Benzoylessigsäure zu Isopelletierin bzw. α‐Phenacyl‐piperidinEuropean Journal of Organic Chemistry, 1959