Synthesis of Peptides Containing ?,?-Disubstituted ?-Amino Acids by the Azirine/Oxazolone Method: The (12-20)-Nonapeptide of the Ionophore Alamethicin-Reference-Cited by-同舟云学术

Synthesis of Peptides Containing ?,?-Disubstituted ?-Amino Acids by the Azirine/Oxazolone Method: The (12-20)-Nonapeptide of the Ionophore Alamethicin

Published:1990-01-31 Issue:1 Volume:73 Page:13-24
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Wipf Peter,Heimgartner Heinz

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference50 articles.

1. A polypeptide antibacterial agent isolated fromTrichoderma viride

2. Action Potentials induced in Biomolecular Lipid Membranes

3. in ?Structure and Activity of Natural Peptides,? Eds. and de Gruyter, Berlin, 1981, p. 75.

4. Alamethicin pore formation: Voltage-dependent flip-flop of ?-helix dipoles

5. Melittin and a chemically modified trichotoxin form alamethicin-type multi-state pores

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