Regioselective palladium-catalyzed olefination of coumarinsvia aerobic oxidative Heck reactions
- 21 November 2012
- journal article
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 49 (2), 196-198
- https://doi.org/10.1039/c2cc37676h
Abstract
Pd-catalyzed oxidative Heck reactions of coumarins were developed via simultaneous C–H functionalization at the C3 position of coumarins under aerobic conditions.Keywords
This publication has 37 references indexed in Scilit:
- Palladium(II)-Catalyzed Dehydrogenative Alkenylation of Cyclic Enaminones via the Fujiwara–Moritani ReactionOrganic Letters, 2011
- Direct Hiyama Cross-Coupling of Enaminones With Triethoxy(aryl)silanes and DimethylphenylsilanolOrganic Letters, 2011
- Palladium‐Catalyzed Regioselective Aerobic Oxidative C-H/N-H Carbonylation of Heteroarenes under Base‐Free ConditionsChemistry – A European Journal, 2011
- Towards mild metal-catalyzed C–H bond activationChemical Society Reviews, 2011
- Intermolecular Dehydrogenative Heck ReactionsChemical Reviews, 2011
- Transition-metal-catalyzed C–C bond formation through the fixation of carbon dioxideChemical Society Reviews, 2011
- Transition-metal catalyzed oxidative cross-coupling reactions to form C–C bonds involving organometallic reagents as nucleophilesChemical Society Reviews, 2011
- Recent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formationChemical Society Reviews, 2011
- Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetateJournal of the American Chemical Society, 1969
- Aromatic substitution of styrene-palladium chloride complexTetrahedron Letters, 1967