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- W2907065590 endingPage "2148" @default.
- W2907065590 startingPage "2144" @default.
- W2907065590 abstract "To show the synthetic utility of palladium/norbornene (Pd/NBE) cooperative catalysis, here we report concise syntheses of indenone-based natural products, pauciflorol F and acredinone A, which are enabled by direct annulation between aryl iodides and unsaturated carboxylic acid anhydrides. Compared to the previous indenone-preparation approaches, this method allows simple aryl iodides to be used as substrates with complete control of the regioselectivity. The total synthesis of acredinone A features two different Pd/NBE-catalyzed ortho acylation reactions for constructing penta-substituted arene cores, including the development of a new ortho acylation/ipso borylation." @default.
- W2907065590 created "2019-01-11" @default.
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- W2907065590 creator A5053319227 @default.
- W2907065590 creator A5057703305 @default.
- W2907065590 date "2019-01-16" @default.
- W2907065590 modified "2023-10-16" @default.
- W2907065590 title "Palladium/Norbornene-Catalyzed Indenone Synthesis from Simple Aryl Iodides: Concise Syntheses of Pauciflorol F and Acredinone A" @default.
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- W2907065590 doi "https://doi.org/10.1002/anie.201813699" @default.
- W2907065590 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6420343" @default.
- W2907065590 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30600880" @default.
- W2907065590 hasPublicationYear "2019" @default.
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