Synlett 2014; 25(14): 2025-2029
DOI: 10.1055/s-0034-1378380
letter
© Georg Thieme Verlag Stuttgart · New York

A Metathesis–Acylation Approach to the Bicyclic Core of Polycyclic Poly­prenylated Acylphloroglucinols

Stefanie Schmitt
a   Institut für Organische Chemie II, Universität des Saarlandes, 66123 Saarbrücken, Germany
,
Eva Feidt
a   Institut für Organische Chemie II, Universität des Saarlandes, 66123 Saarbrücken, Germany
,
David Hartmann
a   Institut für Organische Chemie II, Universität des Saarlandes, 66123 Saarbrücken, Germany
,
Volker Huch
b   Institut für Anorganische Chemie, Universität des Saarlandes, 66123 Saarbrücken, Germany   Fax: +49(681)30264151   Email: j.jauch@mx.uni-saarland.de
,
Johann Jauch*
a   Institut für Organische Chemie II, Universität des Saarlandes, 66123 Saarbrücken, Germany
› Author Affiliations
Further Information

Publication History

Received: 21 March 2014

Accepted after revision: 03 June 2014

Publication Date:
23 July 2014 (online)


Abstract

An approach to a model compound for polycyclic polyprenylated acylphloroglucinols is developed using a ring-closing metathesis approach to give a substituted cyclooctene. This undergoes cyclization via an intramolecular acylation leading to a substituted bicyclo[3.3.1]nonan-9-one related to hyperforin, nemorosone, clusianone, garsubellin A and other members of the polyprenylated acylphloroglucinol.

Supporting Information