Ontology highlight
ABSTRACT:
SUBMITTER: Li Y
PROVIDER: S-EPMC5588696 | biostudies-literature | 2017 Jul
REPOSITORIES: biostudies-literature
Li Yong Y Wei Mufeng M Dai Mingji M
Tetrahedron 20161103 29
A concise approach to synthesize the 5-7-6 tricyclic carbon skeleton of the daphnane/tigliane diterpene natural products has been accomplished <i>via</i> a sequential gold-catalyzed furan formation and furan-allene [4+3] cycloaddition. This work provides new avenues for rapid and diverted synthesis of the medicinally important daphnane/tigliane diterpenes and their unnatural analogues. ...[more]