Efficient Diastereoselective Intermolecular Rhodium-Catalyzed CH 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 CH 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 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
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 CH amination. Good‐to‐excellent yields and excellent diastereoselectivities can be obtained with a stoichiometric amount of the CH bond containing substrate. nttl=N‐1,8‐naphthoyl‐tert‐leucine. |
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ISSN: | 1433-7851 1521-3773 |
DOI: | 10.1002/anie.200601248 |