Diastereoselective Ritter reactions of chiral secondary benzylic alcohols
An acid-catalysed Ritter reaction of chiral secondary benzylic alcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and beta-amino acids.
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2009-01 (16), p.2130-2132 |
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| Hauptverfasser: | , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | An acid-catalysed Ritter reaction of chiral secondary benzylic alcohols enables diastereoselective access to chiral amides, which represent inter alia valuable intermediates for the synthesis of chiral 1,2-diamines and beta-amino acids. |
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| ISSN: | 1359-7345 1364-548X |
| DOI: | 10.1039/b901937e |