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Chiral Tetrafluorobenzobarrelene Ligands for the Rhodium‐Catalyzed Asymmetric Cycloisomerization of Oxygen‐ and Nitrogen‐Bridged 1,6‐Enynes
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2010
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EngineeringOrganic ChemistryChemistryHeterocycle ChemistrySuch DocumentsOrganometallic CatalysisInorganic ChemistryMolecular SciencesBiochemistryDetailed FactsChiral Tetrafluorobenzobarrelene LigandsPharmacologyAsymmetric CatalysisEnantioselective SynthesisBiomolecular EngineeringHeterocyclicNatural SciencesRhodium‐catalyzed Asymmetric CycloisomerizationMain Group ChemistryN- Wie O-heterocyclen
N- wie O-Heterocyclen: Die asymmetrische Cycloisomerisierung von Stickstoff- und Sauerstoff-verbrückten 1,6-Eninen wird durch einen kationischen Rhodiumkomplex mit PPh3 und einem chiralen Dien als Liganden katalysiert. Die Umsetzung liefert chirale 3-Aza- und 3-Oxabicyclo[4.1.0]heptene in hohen Ausbeuten und Enantioselektivitäten. Detailed facts of importance to specialist readers are published as ”Supporting Information”. Such documents are peer-reviewed, but not copy-edited or typeset. They are made available as submitted by the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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