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)
Angew. Chem. Int. Ed. Engl. 41: 4661-4663.

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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. Angew. Chem. Int. Ed. Engl. 2002;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. Angew. Chem. Int. Ed. Engl., 41, 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. Angew. Chem. Int. Ed. Engl. 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. Angew. Chem. Int. Ed. Engl., 41, 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”, Angew. Chem. Int. Ed. Engl., 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. Angew. Chem. Int. Ed. Engl. 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”. Angew. Chem. Int. Ed. Engl. 41 (2002): 4661-4663.
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