| Literature DB >> 28890579 |
Yong Li1, Mufeng Wei2, Mingji Dai1.
Abstract
A concise approach to synthesize the 5-7-6 tricyclic carbon skeleton of the daphnane/tigliane diterpene natural products has been accomplished via 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.Entities:
Keywords: Daphnane/Tigliane; Diterpene; Furan formation; Gold catalysis; [4+3] cycloaddition
Year: 2016 PMID: 28890579 PMCID: PMC5588696 DOI: 10.1016/j.tet.2016.11.005
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457