Selective C‐6 Prenylation of Flavonoids via Europium(III)‐ Catalyzed Claisen Rearrangement and Cross‐Metathesis
- 8 January 2007
- journal article
- Published by Wiley in Advanced Synthesis & Catalysis
- Vol. 349 (1-2), 147-151
- https://doi.org/10.1002/adsc.200600454
Abstract
No abstract availableKeywords
This publication has 49 references indexed in Scilit:
- Prenylated Flavonoids: Pharmacology and BiotechnologyCurrent Medicinal Chemistry, 2005
- A new protocol for benzoannulation by double Claisen rearrangement and ring-closing metathesis reactions as key stepsTetrahedron Letters, 2004
- Combined Multiple Claisen Rearrangement and Ring-closing Metathesis as a Route to Naphthalene, Anthracene, and Anthracycline Ring SystemsChemistry Letters, 2003
- Jüngste Entwicklungen bei der gekreuzten OlefinmetatheseAngewandte Chemie, 2003
- Recent Developments in Olefin Cross‐MetathesisAngewandte Chemie-International Edition, 2003
- Ring-closing metathesis for the synthesis of benzo-fused bicyclic compoundsTetrahedron Letters, 2003
- Flavonoid Function and Activity to Plants and Other OrganismsBiological Sciences in Space, 2003
- Synthesis of Symmetrical Trisubstituted Olefins by Cross MetathesisOrganic Letters, 2002
- An efficient synthesis of the potent phytoestrogens 8-prenylnaringenin and 6-(1,1-dimethylallyl)naringenin by europium(III)-catalyzed Claisen rearrangementTetrahedron, 2001
- Asymmetric O- and C-Alkylation of PhenolsJournal of the American Chemical Society, 1998