Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A

Sewald N (2002)
Angewandte Chemie International Edition 41(24): 4661-4663.

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DOI
Autor*in
Sewald, NorbertUniBi
Einrichtung
Fakultät für Chemie
Erscheinungsjahr
2002
Zeitschriftentitel
Angewandte Chemie International Edition
Band
41
Ausgabe
24
Seite(n)
4661-4663
ISSN
1433-7851
Page URI
https://pub.uni-bielefeld.de/record/1883997

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Sewald N. Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A. Angewandte Chemie International Edition. 2002;41(24):4661-4663.
Sewald, N. (2002). Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A. Angewandte Chemie International Edition, 41(24), 4661-4663. https://doi.org/10.1002/anie.200290008
Sewald, Norbert. 2002. “Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A”. Angewandte Chemie International Edition 41 (24): 4661-4663.
Sewald, N. (2002). Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A. Angewandte Chemie International Edition 41, 4661-4663.
Sewald, N., 2002. Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A. Angewandte Chemie International Edition, 41(24), p 4661-4663.
N. Sewald, “Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A”, Angewandte Chemie International Edition, vol. 41, 2002, pp. 4661-4663.
Sewald, N.: Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A. Angewandte Chemie International Edition. 41, 4661-4663 (2002).
Sewald, Norbert. “Efficient, Racemization-Free Peptide Coupling of N-Alkyl Amino Acids by Using Amino Acid Chlorides Generated In Situ—Total Syntheses of the Cyclopeptides Cyclosporin O and Omphalotin A”. Angewandte Chemie International Edition 41.24 (2002): 4661-4663.

4 Zitationen in Europe PMC

Daten bereitgestellt von Europe PubMed Central.

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9 References

Daten bereitgestellt von Europe PubMed Central.


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Total synthesis of the nematicidal cyclododecapeptide omphalotin A by using racemization-free triphosgene-mediated couplings in the solid phase.
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Sewald, 2002
In situ generation of Fmoc-amino acid chlorides using bis-(trichloromethyl) carbonate and its utilization for difficult couplings in solid-phase peptide synthesis.
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