Publication | Open Access
Antineoplastic Agents. 454. Synthesis of the Strong Cancer Cell Growth Inhibitors <i>trans</i>-Dihydronarciclasine and 7-Deoxy-<i>trans</i>-dihydronarciclasine
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Citations
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References
2009
Year
Bioorganic ChemistryAmaryllidaceae FamilyOrganic ChemistryPharmaceutical ChemistryTumor BiologyMedicinal ChemistryAntineoplastic AgentsCancer Cell BiologyAnti-cancer AgentRadiation OncologyCancer ResearchBiochemistryCancer TreatmentDrug DevelopmentPharmacologyNatural Product SynthesisAsymmetric CatalysisEnantioselective SynthesisAntineoplastic LeadsNatural SciencesMedicinal Plant SpeciesMedicineDerivative (Chemistry)Synthetic ChemistryDrug Discovery
To further pursue the antineoplastic leads offered by our isolation of trans-dihydronarciclasine (1a) and 7-deoxy-trans-dihydronarciclasine (1c) from two medicinal plant species of the Amaryllidaceae family, a practical palladium-catalyzed hydrogenation procedure was developed for the synthesis of these isocarbostyrils from narciclasine (2a) and 7-deoxynarciclasine (2c).
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