Synthetic routes towards enantiomerically pure beta-amino acids

Sewald N (2003)
Angewandte Chemie International Edition 42(47): 5794-5795.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Stichworte
diastereoselectivity; enantioselectivity; Michael addition; amino acids; cycloaddition
Erscheinungsjahr
2003
Zeitschriftentitel
Angewandte Chemie International Edition
Band
42
Ausgabe
47
Seite(n)
5794-5795
ISSN
1433-7851
eISSN
1521-3773
Page URI
https://pub.uni-bielefeld.de/record/1609172

Zitieren

Sewald N. Synthetic routes towards enantiomerically pure beta-amino acids. Angewandte Chemie International Edition. 2003;42(47):5794-5795.
Sewald, N. (2003). Synthetic routes towards enantiomerically pure beta-amino acids. Angewandte Chemie International Edition, 42(47), 5794-5795. https://doi.org/10.1002/anie.200301692
Sewald, Norbert. 2003. “Synthetic routes towards enantiomerically pure beta-amino acids”. Angewandte Chemie International Edition 42 (47): 5794-5795.
Sewald, N. (2003). Synthetic routes towards enantiomerically pure beta-amino acids. Angewandte Chemie International Edition 42, 5794-5795.
Sewald, N., 2003. Synthetic routes towards enantiomerically pure beta-amino acids. Angewandte Chemie International Edition, 42(47), p 5794-5795.
N. Sewald, “Synthetic routes towards enantiomerically pure beta-amino acids”, Angewandte Chemie International Edition, vol. 42, 2003, pp. 5794-5795.
Sewald, N.: Synthetic routes towards enantiomerically pure beta-amino acids. Angewandte Chemie International Edition. 42, 5794-5795 (2003).
Sewald, Norbert. “Synthetic routes towards enantiomerically pure beta-amino acids”. Angewandte Chemie International Edition 42.47 (2003): 5794-5795.

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