Rauwolfia alkaloids XXVI. Stereochemistry at C-17
- 1 July 1956
- journal article
- Published by Springer Nature in Cellular and Molecular Life Sciences
- Vol. 12 (7) , 250-251
- https://doi.org/10.1007/bf02157329
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- THE STEREOCHEMICAL FORMULATION OF RESERPINEJournal of the American Chemical Society, 1955
- The constitution of the alloyohimbanesCellular and Molecular Life Sciences, 1955
- Rauwolfia alkaloids XXI. The stereochemistry of reserpine and deserpidineCellular and Molecular Life Sciences, 1955
- Rauwolfia Alkaloids. XIX.1 The Constitution of Deserpidine and ReserpineJournal of the American Chemical Society, 1955
- RAUWOLFIA ALKALOIDS. XXII. FURTHER OBSERVATIONS OF THE STEREOCHEMISTRY OF RESERPINEJournal of the American Chemical Society, 1955
- Rauwolfia Alkaloids. XVII. 3-Epi-α-yohimbineJournal of the American Chemical Society, 1955
- The molecular rotations of polycyclic compounds. Part III. Polycyclic alcohols and their derivativesJournal of the Chemical Society, 1954
- The Structure of Isorubijervine. Conversion to Solanidane and Solanidane-3β-ol1Journal of the American Chemical Society, 1953
- The Action of Alcoholic Potassium Hydroxide on ▵16-20-Ketosteroids1Journal of the American Chemical Society, 1951