Abstract
Borylated functional π-systems are useful building blocks to enable efficient synthesis of novel molecular architectures with beautiful structures, intriguing properties and unique functions. Introduction of boronic ester substituents to a variety of extended πsystems can be achieved through either iridium-catalyzed direct C-H borylation or the two-step procedure via electrophilic halogenation followed by palladium-catalyzed borylation. This review article focuses on our recent progress on borylation of large πconjugated systems such as porphyrins, perylene bisimides, hexabenzocoronenes and dipyrrins. © 2014 The Japan Academy.
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CITATION STYLE
Shinokubo, H. (2014, January). Transition metal catalyzed borylation of functional π-systems. Proceedings of the Japan Academy Series B: Physical and Biological Sciences. https://doi.org/10.2183/pjab.90.1
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