anhydrolycorinone has been researched along with hippadine* in 2 studies
2 other study(ies) available for anhydrolycorinone and hippadine
Article | Year |
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A domino amidation route to indolines and indoles: rapid syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine.
[reaction: see text] When subjected to palladium-catalyzed amidation conditions, 2-triflyloxy phenethyl carbonates undergo, in addition to the expected aryl cross-coupling, an additional amidation with net displacement of the carbonate. The result is a one-step synthesis of indolines which may be oxidized to indoles. The utility of the procedure is illustrated by the two- or three-step syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine. Topics: Alkaloids; Amaryllidaceae Alkaloids; Amides; Catalysis; Indole Alkaloids; Indoles; Molecular Structure; Oxidation-Reduction; Phenanthridines | 2005 |
Total synthesis of Amaryllidaceae alkaloids utilizing sequential intramolecular heterocyclic azadiene Diels-Alder reactions of an unsymmetrical 1,2,4,5-tetrazine.
Convergent total syntheses of anhydrolycorinone, hippadine, and anhydrolycorinium chloride are detailed, enlisting sequential inverse electron demand Diels-Alder reactions of an unsymmetrical N-acyl-6-amino-1,2,4,5-tetrazine. Topics: Alkaloids; Amaryllidaceae Alkaloids; Heterocyclic Compounds; Indicators and Reagents; Phenanthridines; Plants, Medicinal | 2000 |