2,6-Bis(pyrazol-1-yl)pyridine cobalt-catalyzed high selective hydroboration of alkenes
•A series of novel 2,6-bis(pyrazol-1-yl)pyridine Cobalt complexes have been synthesized and applied to catalyze the highly selective hydroboronation of alkenes.•These catalysts function effectively under mild, solvent-free conditions, demonstrating contrasting selectivities: Markovnikov-type selecti...
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Veröffentlicht in: | Molecular catalysis 2024-11, Vol.568, p.114516, Article 114516 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •A series of novel 2,6-bis(pyrazol-1-yl)pyridine Cobalt complexes have been synthesized and applied to catalyze the highly selective hydroboronation of alkenes.•These catalysts function effectively under mild, solvent-free conditions, demonstrating contrasting selectivities: Markovnikov-type selectivity for vinylarenes and anti-Markovnikov-type selectivity for alkyl alkenes.
A novel series of cobalt (II) catalysts featuring 2,6-bis(pyrazol-1-yl)pyridine ligands have been synthesized for the purpose of achieving high selectivity in hydroboration reactions of alkenes. These catalysts function effectively under mild, solvent-free conditions, demonstrating contrasting selectivities: Markovnikov-type selectivity for vinylarenes and anti-Markovnikov-type selectivity for alkyl alkenes. This dual-selectivity system offers a versatile platform for the controlled hydroboration of a diverse range of alkene substrates.
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ISSN: | 2468-8231 2468-8231 |
DOI: | 10.1016/j.mcat.2024.114516 |