Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances

Sewald N (1996)
Amino Acids 11(3): 397-408.

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DOI
Autor*in
Sewald, NorbertUniBi
Einrichtung
Fakultät für Chemie > Organische Chemie III
Erscheinungsjahr
1996
Zeitschriftentitel
Amino Acids
Band
11
Ausgabe
3
Seite(n)
397-408
ISSN
0939-4451
Page URI
https://pub.uni-bielefeld.de/record/1864923

Zitieren

Sewald N. Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances. Amino Acids. 1996;11(3):397-408.
Sewald, N. (1996). Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances. Amino Acids, 11(3), 397-408. https://doi.org/10.1007/BF00807944
Sewald, Norbert. 1996. “Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances”. Amino Acids 11 (3): 397-408.
Sewald, N. (1996). Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances. Amino Acids 11, 397-408.
Sewald, N., 1996. Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances. Amino Acids, 11(3), p 397-408.
N. Sewald, “Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances”, Amino Acids, vol. 11, 1996, pp. 397-408.
Sewald, N.: Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances. Amino Acids. 11, 397-408 (1996).
Sewald, Norbert. “Stereoselective Synthesis of beta-Amino Acids via Conjugate Addition of Nitrogen Nucleophiles to alpha,beta-Unsaturated Esters - Recent Advances”. Amino Acids 11.3 (1996): 397-408.

7 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

Acidic-functionalized ionic liquid as an efficient, green and reusable catalyst for hetero-Michael addition of nitrogen, sulfur and oxygen nucleophiles to α,β-unsaturated ketones.
Han F, Yang L, Li Z, Xia C., Org Biomol Chem 10(2), 2012
PMID: 22076060
Structural diversity of bicyclic amino acids.
Trabocchi A, Scarpi D, Guarna A., Amino Acids 34(1), 2008
PMID: 17701095
Stereoselective synthesis of beta-amino acids.
Guo HS, Zhao HJ, Niu DQ, Zhao K., J Asian Nat Prod Res 7(2), 2005
PMID: 15621613
Beta2-amino acids-syntheses, occurrence in natural products, and components of beta-peptides1,2.
Lelais G, Seebach D., Biopolymers 76(3), 2004
PMID: 15148683
Side-chain control of beta-peptide secondary structures.
Martinek TA, Fülöp F., Eur J Biochem 270(18), 2003
PMID: 12950249
Design and synthesis of a beta-amino phosphotyrosyl mimetic suitably protected for peptide synthesis.
Lee K, Zhang M, Yang D, Burke TR., Bioorg Med Chem Lett 12(23), 2002
PMID: 12419370
Design and synthesis of inhibitors incorporating beta -amino acids of metalloendopeptidase EC 3.4.24.15.
Steer DL, Lew RA, Perlmutter P, Smith AI, Aguilar MI., J Pept Sci 6(9), 2000
PMID: 11016884

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