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- W2467926383 endingPage "12175" @default.
- W2467926383 startingPage "12166" @default.
- W2467926383 abstract "Abstract Palladium‐catalysed coupling reactions based on a novel and easy‐to‐synthesise difluorinated organotrifluoroborate were used to assemble precursors to 6π‐electrocyclisations of three different types. Electrocyclisations took place at temperatures between 90 and 240 °C, depending on the central component of the π‐system; nonaromatic trienes were most reactive, but even systems that required the temporary dearomatisation of two arenyl subunits underwent electrocyclisation, albeit at elevated temperatures. Photochemical conditions were effective for these more demanding reactions. The package of methods delivered a structurally diverse set of fluorinated arenes, spanning a 20 kcal mol −1 range of reactivity, by a flexible route." @default.
- W2467926383 created "2016-07-22" @default.
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- W2467926383 creator A5082342124 @default.
- W2467926383 creator A5090875682 @default.
- W2467926383 date "2016-07-14" @default.
- W2467926383 modified "2023-09-27" @default.
- W2467926383 title "Modular Construction of Fluoroarenes from a New Difluorinated Building Block by Cross-Coupling/Electrocyclisation/Dehydrofluorination Reactions" @default.
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