Pd‐Catalysed Diastereoselective Synthesis of aza‐Spirocyclic P‐Stereogenic Phosphine Oxides
Phosphine oxides and spirocyclic compounds are privileged molecules widely employed in a variety of catalytic transformations either as chiral ligands for metals or bifunctional organocatalysts. Herein, we developed a Pd‐catalysed cross‐coupling reaction to synthesize spirocyclic amino‐phosphine oxi...
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Veröffentlicht in: | European journal of organic chemistry 2023-06, Vol.26 (24), p.n/a |
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Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Phosphine oxides and spirocyclic compounds are privileged molecules widely employed in a variety of catalytic transformations either as chiral ligands for metals or bifunctional organocatalysts. Herein, we developed a Pd‐catalysed cross‐coupling reaction to synthesize spirocyclic amino‐phosphine oxides with a P‐stereogenic centre which could serve as potential P*(O), N‐ligands or organocatalysis.
We designed a Pd‐catalyzed cross‐coupling reaction to synthesize diastereoselective spirocyclic amino‐phosphine oxides with a P‐stereogenic center. These potential P*(O), N‐ligands contain both electronic donor and H donor/acceptor properties, which may be used to promote asymmetric catalytic reactions with high selectivity and efficiency. |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.202300265 |