Total synthesis of Amaryllidaceae alkaloids utilizing sequential intramolecular heterocyclic azadiene Diels-Alder reactions of an unsymmetrical 1,2,4,5-tetrazine
Dl. Boger et Se. Wolkenberg, Total synthesis of Amaryllidaceae alkaloids utilizing sequential intramolecular heterocyclic azadiene Diels-Alder reactions of an unsymmetrical 1,2,4,5-tetrazine, J ORG CHEM, 65(26), 2000, pp. 9120-9124
Convergent total syntheses of anhydrolycorinone, hippadine, and anhydrolyco
rinium chloride are detailed, enlisting sequential inverse electron demand
Diels-Alder reactions of an unsymmetrical N-acyl-6-amino-1,2,4,5-tetrazine.