Organic Letters · 2019 · 16 citations · 34 references
Natural SciencesChemistryCatalysisOrganic ChemistryOrganometallic ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisAlkane FunctionalizationAlkylation ReactionsElectron-donating GroupsHeterocycle Functionalization
We report a phosphine-mediated direct β-acylation of α,β-unsaturated 1,3-diketones with acyl chlorides and a base. Functionalized furanones were also prepared by the reaction of cinnamic acid and acyl chloride according to our protocol via β-acylation. Our studies revealed that α,β-unsaturated 1,3-diketones with an electron-donating group at the second position favor the formation of β-acylated products, whereas those with oxygen, such as anhydrides, favor furanones via an unprecedented C-acylation/cyclization sequence.
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Nucleophilic Phosphine Organocatalysis
Joey L. Methot, William Roush · Advanced Synthesis & Catalysis · 2004 · 969 citations · Full text
Sean P. Brown, Nicole C. Goodwin, David W. C. MacMillan · Journal of the American Chemical Society · 2003 · 446 citations
Ligand-accelerated non-directed C–H functionalization of arenes
Peng Wang, Pritha Verma, Guoqin Xia et al. · Nature · 2017 · 437 citations · Full text