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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DOI
Autor*in
Sewald, NorbertUniBi
Einrichtung
Fakultät für Chemie > Organische Chemie III
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.

12 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

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PMID: 24014472
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Knapp JM, Zhu JS, Wood AB, Kurth MJ., ACS Comb Sci 14(2), 2012
PMID: 22181856
Synthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines.
Nonn M, Kiss L, Sillanpää R, Fülöp F., Beilstein J Org Chem 8(), 2012
PMID: 22423276
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Fustero S, del Pozo C, Mulet C, Lazaro R, Sánchez-Roselló M., Chemistry 17(50), 2011
PMID: 22083999
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Niphakis MJ, Turunen BJ, Georg GI., J Org Chem 75(20), 2010
PMID: 20929269
Enantioselective Michael addition of alpha-substituted cyanoacetates to vinyl ketones catalyzed by bifunctional organocatalysts.
Liu TY, Li R, Chai Q, Long J, Li BJ, Wu Y, Ding LS, Chen YC., Chemistry 13(1), 2007
PMID: 17039561
Preparation of chiral derivatives of beta-Ala containing the alpha-phenylethyl group: useful starting materials for the asymmetric synthesis of beta-amino acids.
Guzmán-Mejía R, Reyes-Rangel G, Juaristi E., Nat Protoc 2(11), 2007
PMID: 18007611

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Daten bereitgestellt von Europe PubMed Central.

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