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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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. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c7cc00997f |