| Literature DB >> 26273110 |
Daniel Knueppel, Jingyue Yang1, Bo Cheng, Douglas Mans, Stephen F Martin1.
Abstract
A total synthesis of the aglycone of IB-00208 was accomplished in 22 steps using a newly developed approach towards polycyclic 1,4-dioxygenated xanthones from benzocyclobutenones. The generality of this entry to xanthones was initially established on several model systems before it was successfully applied to the construction of the hexacyclic core of the natural product. A new and potentially general approach towards angularly-fused benzocyclobutenones using ring-closing metathesis (RCM) was also developed.Entities:
Keywords: Moore rearrangement; cyclobutenediones; natural products; polycyclic xanthones; total synthesis
Year: 2015 PMID: 26273110 PMCID: PMC4528365 DOI: 10.1016/j.tet.2015.05.024
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457