The first total synthesis of efrapeptin C
Jost M, Greie JC, Stemmer N, Wilking SD, Altendorf K, Sewald N (2002)
Angewandte Chemie International Edition 41(22): 4267-4269.
Zeitschriftenaufsatz
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Autor*in
Jost, M;
Greie, JC;
Stemmer, N;
Wilking, SD;
Altendorf, K;
Sewald, NorbertUniBi
Einrichtung
Stichworte
efrapeptins;
alpha-aminoisobutyric acid;
total synthesis;
peptides;
synthesis;
solid-phase
Erscheinungsjahr
2002
Zeitschriftentitel
Angewandte Chemie International Edition
Band
41
Ausgabe
22
Seite(n)
4267-4269
ISSN
1433-7851
eISSN
1521-3773
Page URI
https://pub.uni-bielefeld.de/record/1613075
Zitieren
Jost M, Greie JC, Stemmer N, Wilking SD, Altendorf K, Sewald N. The first total synthesis of efrapeptin C. Angewandte Chemie International Edition. 2002;41(22):4267-4269.
Jost, M., Greie, J. C., Stemmer, N., Wilking, S. D., Altendorf, K., & Sewald, N. (2002). The first total synthesis of efrapeptin C. Angewandte Chemie International Edition, 41(22), 4267-4269. https://doi.org/10.1002/1521-3773(20021115)41:22<4267::AID-ANIE4267>3.0.CO;2-K
Jost, M, Greie, JC, Stemmer, N, Wilking, SD, Altendorf, K, and Sewald, Norbert. 2002. “The first total synthesis of efrapeptin C”. Angewandte Chemie International Edition 41 (22): 4267-4269.
Jost, M., Greie, J. C., Stemmer, N., Wilking, S. D., Altendorf, K., and Sewald, N. (2002). The first total synthesis of efrapeptin C. Angewandte Chemie International Edition 41, 4267-4269.
Jost, M., et al., 2002. The first total synthesis of efrapeptin C. Angewandte Chemie International Edition, 41(22), p 4267-4269.
M. Jost, et al., “The first total synthesis of efrapeptin C”, Angewandte Chemie International Edition, vol. 41, 2002, pp. 4267-4269.
Jost, M., Greie, J.C., Stemmer, N., Wilking, S.D., Altendorf, K., Sewald, N.: The first total synthesis of efrapeptin C. Angewandte Chemie International Edition. 41, 4267-4269 (2002).
Jost, M, Greie, JC, Stemmer, N, Wilking, SD, Altendorf, K, and Sewald, Norbert. “The first total synthesis of efrapeptin C”. Angewandte Chemie International Edition 41.22 (2002): 4267-4269.
Daten bereitgestellt von European Bioinformatics Institute (EBI)
6 Zitationen in Europe PMC
Daten bereitgestellt von Europe PubMed Central.
Solution synthesis, conformational analysis, and antimicrobial activity of three alamethicin F50/5 analogs bearing a trifluoroacetyl label.
De Zotti M, Ballano G, Jost M, Salnikov ES, Bechinger B, Oancea S, Crisma M, Toniolo C, Formaggio F., Chem Biodivers 11(8), 2014
PMID: 25146762
De Zotti M, Ballano G, Jost M, Salnikov ES, Bechinger B, Oancea S, Crisma M, Toniolo C, Formaggio F., Chem Biodivers 11(8), 2014
PMID: 25146762
Conformational properties of secondary amino acids: replacement of pipecolic acid by N-methyl-l-alanine in efrapeptin C.
Dutt Konar A, Vass E, Hollósi M, Majer Z, Grüber G, Frese K, Sewald N., Chem Biodivers 10(5), 2013
PMID: 23681735
Dutt Konar A, Vass E, Hollósi M, Majer Z, Grüber G, Frese K, Sewald N., Chem Biodivers 10(5), 2013
PMID: 23681735
Synthesis and conformational analysis of efrapeptins.
Weigelt S, Huber T, Hofmann F, Jost M, Ritzefeld M, Luy B, Freudenberger C, Majer Z, Vass E, Greie JC, Panella L, Kaptein B, Broxterman QB, Kessler H, Altendorf K, Hollósi M, Sewald N., Chemistry 18(2), 2012
PMID: 22147615
Weigelt S, Huber T, Hofmann F, Jost M, Ritzefeld M, Luy B, Freudenberger C, Majer Z, Vass E, Greie JC, Panella L, Kaptein B, Broxterman QB, Kessler H, Altendorf K, Hollósi M, Sewald N., Chemistry 18(2), 2012
PMID: 22147615
Interruption of a 3(10)-helix by a single Gly residue in a poly-Aib motif: a crystallographic study.
Solà J, Helliwell M, Clayden J., Biopolymers 95(1), 2011
PMID: 20725951
Solà J, Helliwell M, Clayden J., Biopolymers 95(1), 2011
PMID: 20725951
Synthesis of the orthogonally protected amino alcohol Phaol and analogs.
Nelissen J, Nuyts K, Dehaen W, De Borggraeve WM., J Pept Sci 17(7), 2011
PMID: 21491546
Nelissen J, Nuyts K, Dehaen W, De Borggraeve WM., J Pept Sci 17(7), 2011
PMID: 21491546
Trypsin-catalyzed synthesis of dipeptide containing alpha-aminoisobutyric acid using p- and m-(amidinomethyl)phenyl esters as acyl donor.
Sekizaki H, Itoh K, Shibuya A, Toyota E, Kojoma M, Tanizawa K., Chem Pharm Bull (Tokyo) 56(5), 2008
PMID: 18451559
Sekizaki H, Itoh K, Shibuya A, Toyota E, Kojoma M, Tanizawa K., Chem Pharm Bull (Tokyo) 56(5), 2008
PMID: 18451559
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Daten bereitgestellt von Europe PubMed Central.
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