The alkaloids of Lycopodium cernuum L. II. The stereochemistry of cernuine and lycocernuine
- 1 March 1967
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 45 (5) , 445-450
- https://doi.org/10.1139/v67-078
Abstract
The relative stereochemistries of cernuine (I) and lycocernuine (n) have been derived by a combination of chemical and physical methods. Evidence is presented which indicates that I and II also represent the absolute stereochemistry of these alkaloids. The stereochemistry of allocernuine is discussed, and the isomerization of allocernuine into epiallocernuine is described.This publication has 7 references indexed in Scilit:
- The alkaloids of Lycopodium cernuum L. I. The structures of cernuine and lycocernuineCanadian Journal of Chemistry, 1967
- The alkaloids of Lycopodium cernuum L. III. The synthesis of dihydrodeoxyepiallocernuineCanadian Journal of Chemistry, 1967
- Azabicyclic Alcohols. I. Stereochemistry of the Hydroxyquinolizidines1The Journal of Organic Chemistry, 1964
- Reaction of Nitrosyl Chloride with Steroid 5-Enes.1 Nuclear Magnetic Resonance as a Stereochemical Tool in SteroidsThe Journal of Organic Chemistry, 1964
- Determination des configurations par “dedoublement partiel”—IIITetrahedron, 1964
- Configurational and conformational analysisTetrahedron, 1963
- Unsaturated Amines. XII. Steric Requirements of Mercuric Acetate Oxidation of Tertiary Amines1Journal of the American Chemical Society, 1958