Synthesis of Highly Substituted 1,3-Dienes and 1,3,5-Trienes by the Palladium-Catalyzed Coupling of Vinylic Halides, Internal Alkynes, and Organoboranes
- 24 July 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (17), 2993-2996
- https://doi.org/10.1021/ol0348349
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- An Efficient, Regio- and Stereoselective Palladium-Catalyzed Route to Tetrasubstituted OlefinsOrganic Letters, 2003
- Synthetic methodologies for carbo-substituted conjugated dienesRussian Chemical Reviews, 2001
- Synthesis of Coumarins via Palladium-Catalyzed Carbonylative Annulation of Internal Alkynes by o-IodophenolsOrganic Letters, 2000
- Highly Regio- and Stereoselective Acylboration of Allenes Catalyzed by Palladium Complexes: An Efficient Route to a New Class of 2-AcylallylboronatesJournal of the American Chemical Society, 2000
- Transition Metal-Catalyzed Carbocyclizations in Organic SynthesisChemical Reviews, 1996
- Palladium-Catalyzed Cross-Coupling Reactions of Organoboron CompoundsChemical Reviews, 1995
- Fluoride-Mediated Boronic Acid Coupling ReactionsThe Journal of Organic Chemistry, 1994
- Synthesis of indenones via palladium-catalyzed annulation of internal alkynesThe Journal of Organic Chemistry, 1993
- Synthesis of indoles via palladium-catalyzed heteroannulation of internal alkynesJournal of the American Chemical Society, 1991
- Transition metal-mediated cycloaddition reactions of alkynes in organic synthesisChemical Reviews, 1988