Exhaustive Suzuki-Miyaura reactions of polyhalogenated heteroarenes with alkyl boronic pinacol estersElectronic supplementary information (ESI) available: Full experimental details, copies of NMR spectra (PDF). See DOI: 10.1039/c7cc00997f

A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that ena...

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Hauptverfasser: Laulhé, Sébastien, Blackburn, J. Miles, Roizen, Jennifer L
Format: Artikel
Sprache:eng
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Zusammenfassung:A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines. This method facilitates a formal synthesis of normuscopyridine and the rapid assembly of a dumbbell shaped portion of a [2]rotaxane. A novel Suzuki-Miyaura protocol is described that enables the exhaustive alkylation of polychlorinated pyridines.
ISSN:1359-7345
1364-548X
DOI:10.1039/c7cc00997f