Isolation, Structure Determination, and Biological Activity of a Novel Alkaloid, Perophoramidine, from the Philippine Ascidian Perophora namei
The Journal of Organic Chemistry2002Vol. 67(20), pp. 7124–7126
Citations Over TimeTop 10% of 2002 papers
Abstract
Chemical investigation of the Philippine ascidian Perophora namei has resulted in the isolation of a novel polycyclic alkaloid, perophoramidine (1). The structure of 1 was determined by the interpretation of 1D/2D NMR and MS data. Dehalogenation of perophoramidine (1) by ammonium formate catalyzed transfer hydrogenation confirmed the type and number of halogen atoms present in 1.
Related Papers
- → A mild and efficient method for bromination of alcohols using α,α-dibromo-β-dicarbonyl compounds as halogen sources(2013)13 cited
- → Reactivity of α-arylseleno-aldehydes towards halogens and benzeneselenenyl chloride(1988)18 cited
- → Salts of symmetric polynitropentanes and their reactions with halogens(1983)
- → ChemInform Abstract: BROMINATION OF METHYL TRANS‐CINNAMATE IN HYDROXYLIC SOLVENTS(1974)
- → ChemInform Abstract: Reactions of Polyfluoro‐β‐ketocarboxylic Acid Esters and Their α‐Halogen Derivatives with Phosphorus Pentachloride.(1988)