Highly Convergent Total Synthesis of (+)-Lithospermic Acid via a Late-Stage Intermolecular C−H Olefination
- 28 March 2011
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 133 (15), 5767-5769
- https://doi.org/10.1021/ja2010225
Abstract
The total synthesis of (+)-lithospermic acid is reported, which exploits two successive C−H activation reactions as key steps. Rh-catalyzed carbene C−H insertion reaction utilizing Davies’s catalyst was used to forge dihydrobenzofuran core, and a late-stage intermolecular C−H olefination coupled the olefin unit with the dihydrobenzofuran core to construct the molecule in a highly convergent manner.Keywords
This publication has 28 references indexed in Scilit:
- Ligand-Accelerated C−H Activation Reactions: Evidence for a Switch of MechanismJournal of the American Chemical Society, 2010
- Constructing Multiply Substituted Arenes Using Sequential Palladium(II)‐Catalyzed C-H OlefinationAngewandte Chemie International Edition, 2010
- Ligand-Enabled Reactivity and Selectivity in a Synthetically Versatile Aryl C–H OlefinationScience, 2010
- Rhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond ActivationChemical Reviews, 2009
- Total Synthesis of (±)-Rhazinal Using Novel Palladium-Catalyzed CyclizationsThe Journal of Organic Chemistry, 2009
- Explorations into Neolignan Biosynthesis: Concise Total Syntheses of Helicterin B, Helisorin, and Helisterculin A from a Common IntermediateJournal of the American Chemical Society, 2009
- Reassignment of the Configuration of Salvianolic Acid B and Establishment of Its Identity with Lithospermic Acid BJournal of Natural Products, 2006
- Stereocontrolled Total Synthesis of (−)-Ephedradine A (Orantine)Journal of the American Chemical Society, 2003
- Total synthesis of heptamethyl lithospermateThe Journal of Organic Chemistry, 1979
- Lithospermum ruderale: Partial characterization of the principal polyphenol isolated from the rootsPhytochemistry, 1963