Part. IV - Obtention de nouveaux squelettes diterpeniques tetracycliques lors d'isomerisation d'epoxydes-8,9 diterpeniques
作者:M. Taran、B. Delmond
DOI:10.1016/s0040-4020(01)82060-3
日期:1986.1
been studied. We report a rearrangement of tetrasubstituted epoxide leading to new tetracyclic diterpene skeletons. The nature of the bicyclo[3.2.1] octane moiety constituting the C/D ring system means that these new compounds could be related to stemodane and stemarane diterpenes. These rearrangements could provide a chemical test for the biosynthesis of aphidicolin derivatives.