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.

Zeitschriftenaufsatz | Veröffentlicht | Englisch
 
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Stichworte
coupling reagent; amino acids; bioorganic chemistry; synthesis; triphosgene; total; peptides
Erscheinungsjahr
2002
Zeitschriftentitel
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Band
41
Ausgabe
24
Seite(n)
4661-4663
ISSN
1433-7851
eISSN
1521-3773
Page URI
https://pub.uni-bielefeld.de/record/1612899

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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. doi:10.1002/anie.200290008
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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