Catalytic Olefin Transpositions Facilitated by Ruthenium N,N,N-Pincer Complexes

In this report, we demonstrate olefin transposition/isomerization reactions catalyzed by a series of N,N,N-pincer (1,3-bis­(2-pyridylimino)­isoindoline) Ru-hydride complexes. The protocol proceeds at room temperature for most substrates, achieving excellent yields, regioselectivity, and diastereosel...

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Veröffentlicht in:Journal of organic chemistry 2024-07, Vol.89 (13), p.9647-9653
Hauptverfasser: Davies, Alex M., Greene, Kara H., Allen, Anthony R., Farris, Benjamin M., Szymczak, Nathaniel K., Stephenson, Corey R. J.
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Sprache:eng
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Zusammenfassung:In this report, we demonstrate olefin transposition/isomerization reactions catalyzed by a series of N,N,N-pincer (1,3-bis­(2-pyridylimino)­isoindoline) Ru-hydride complexes. The protocol proceeds at room temperature for most substrates, achieving excellent yields, regioselectivity, and diastereoselectivity in short reaction times. The air-stable Ru-chloride derivatives of these complexes exhibit comparable reactivity enabling benchtop setup and synthetic versatility. Furthermore, we demonstrate the potential for one-pot cascade sequences of the products derived from the transposition reactions.
ISSN:0022-3263
1520-6904
1520-6904
DOI:10.1021/acs.joc.4c00304