Synthesis and conformational studies of peptides containing TOAC, a spin-labelled Cα,α-disubstituted glycine-Reference-Cited by-同舟云学术

Synthesis and conformational studies of peptides containing TOAC, a spin-labelled Cα,α-disubstituted glycine

Published:1995-01 Issue:1 Volume:1 Page:45-57
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Peptide Sci.

Author:

Toniolo Claudio,Valente Ezio,Formaggio Fernando,Crisma Marco,Pilloni Giuseppe,Corvaja Carlo,Toffoletti Antonio,Martinez Gary V.,Hanson M. Paul,Millhauser Glenn L.,George Clifford,Flippen-Anderson Judith L.

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference48 articles.

1. Structures of polypeptides from α-amino acids disubstituted at the α-carbon

2. Stereochemically constrained peptides. Theoretical and experimental studies on the conformations of peptides containing 1-aminocyclohexanecarboxylic acid

3. Structural versatility of peptides from C.alpha.,.alpha.-dialkylated glycines. A conformational energy computation and x-ray diffraction study of homopeptides from 1-aminocyclohexane-1-carboxylic acid1

4. Structural versatility of peptides from C.alpha.,.alpha.-dialkylated glycines. An infrared absorption and 1H nuclear magnetic resonance study of homopeptides from 1-aminocyclohexane-1-carboxylic acid1

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