Efficient Diastereoselective Intermolecular Rhodium-Catalyzed CH Amination

Successful matchmaking: The combination of a chiral nitrene precursor with a chiral rhodium(II) catalyst is the key factor that allows efficient intermolecular regioselective CH amination. Good‐to‐excellent yields and excellent diastereoselectivities can be obtained with a stoichiometric amount of...

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Veröffentlicht in:Angewandte Chemie International Edition 2006-07, Vol.45 (28), p.4641-4644
Hauptverfasser: Liang, Chungen, Robert-Peillard, Fabien, Fruit, Corinne, Müller, Paul, Dodd, Robert H., Dauban, Philippe
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Sprache:eng
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Zusammenfassung:Successful matchmaking: The combination of a chiral nitrene precursor with a chiral rhodium(II) catalyst is the key factor that allows efficient intermolecular regioselective CH amination. Good‐to‐excellent yields and excellent diastereoselectivities can be obtained with a stoichiometric amount of the CH bond containing substrate. nttl=N‐1,8‐naphthoyl‐tert‐leucine.
ISSN:1433-7851
1521-3773
DOI:10.1002/anie.200601248