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- Determination of vincamine in plasma by high-performance liquid chromatography with voltammetric detection. Malcolm R. Smyth
, Analyst
, 1986
, 111
, 851
- X-Ray determination of the molecular structure and absolute configuration of vincamine and of its hydrobromide methanolate. Hans Peter Weber, Trevor J. Petcher
, J. Chem. Soc., Perkin Trans. 2
, 1973
, 2001
- Dye-sensitized photo-oxygenation of the Aspidosperma alkaloids vincadifformine and tabersonine. A new, convenient approach to vincamine. Luisella Calabi, Bruno Danieli, Giordano Lesma, Giovanni Palmisano
, J. Chem. Soc., Perkin Trans. 1
, 1982
, 1371
- Total synthesis of (±)-vincamine. K. H. Gibson, J. E. Saxton
, J. Chem. Soc. D
, 1969
, 1490
- Synthetic approach to (±)-vincamine via cleavage of an α-diketone monothioacetal. Alternative synthesis of (±)-eburnamine, (±)-isoeburnamine, and (±)-eburnamenine. Seiichi Takano, Susumi Hatakeyama, Kunio Ogasawara
, J. Chem. Soc., Perkin Trans. 1
, 1980
, 457
- Ozonation in alkoloid chemistry: a mild and selective conversion of vincadifformine into vincamine. Bruno Danieli, Giordano Lesma, Giovanni Palmisano, Bruno Gabetta
, J. Chem. Soc., Chem. Commun.
, 1981
, 908
- A new asymmetric route to (+)-vincamine. Seiichi Takano, Seiji Sato, Emiko Goto, Kunio Ogasawara
, J. Chem. Soc., Chem. Commun.
, 1986
, 156
- Discovery of a P450-catalyzed step in vindoline biosynthesis: a link between the aspidosperma and eburnamine alkaloids. Franziska Kellner, Fernando Geu-Flores, Nathaniel H. Sherden, Stephanie Brown, Emilien Foureau, Vincent Courdavault, Sarah E. O'Connor
, Chem. Commun.
, 2015
, 51
, 7626
- Synthesis of Vinca alkaloids and related compounds. Part 18. Stereochemical investigations on some intermediates leading to (+)-vincamine. Lajos Szabó, Pál Kolonits, György Kalaus, Csaba Szántay, Alajos Kálmán, László Párkálnyi, Márton Kajtár, János Ángyán
, J. Chem. Soc., Perkin Trans. 2
, 1984
, 1629
- Stereodivergent routes in organic synthesis: carbohydrates, amino acids, alkaloids and terpenes. Carmen Nájera, Francisco Foubelo, José M. Sansano, Miguel Yus
, Org. Biomol. Chem.
, 2020
, 18
, 1232