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- W2291597218 endingPage "3093" @default.
- W2291597218 startingPage "3084" @default.
- W2291597218 abstract "On the basis of a threefold borylated truxene, which is accessible in high yields by iridium-catalyzed borylation under CH-activation, fused π-extended truxenes have been synthesized by a two-step method of first Suzuki-Miyaura cross-coupling reaction and subsequent condensation reaction. The mild condensation method tolerates the presence of a variety of functional groups, such as nitro, fluoro, or carboxyl moieties. Furthermore, by using this approach, N- and S-heteroarene analogues become accessible for the first time, as well as larger structures that represent derivatives of precursors for fullerene C60 or buckybowls. The attached tert-butyl groups make all derivatives sufficiently soluble to allow full spectroscopic and electrochemical investigations. Postfunctionalization of selected derivatives for further synthetic applications of the compounds is also presented." @default.
- W2291597218 created "2016-06-24" @default.
- W2291597218 creator A5043398784 @default.
- W2291597218 creator A5077936026 @default.
- W2291597218 creator A5084670164 @default.
- W2291597218 date "2016-02-02" @default.
- W2291597218 modified "2023-10-06" @default.
- W2291597218 title "Fused π-Extended Truxenes via a Threefold Borylation as the Key Step" @default.
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