Radical cyclisations onto 2 (5H)-furanone and maleate electrophores. An approach to the spiro-and linear-fused γ-lactone ring systems found in the ginkgolides
T Harrison, PL Myers, G Pattenden
文献索引:Harrison, Timothy; Myers, Peter L.; Pattenden, Gerald Tetrahedron, 1989 , vol. 45, # 16 p. 5247 - 5262
Intramolecular radical cyclisations involving α-acetal methyl centres, and 2 (5H)-furanone and maleate electrophores, allow the facile synthesis of spiro-and linear-fused γ-lactone ring systems eg (5),(6),(7) and (8) present in the 'ginkgolides' viz (1) and (2) produced by the ginkgo tree Ginkgo biloba.