The design and synthesis of mimetics of peptide β-turns
- 1 April 1988
- journal article
- research article
- Published by Wiley in Journal of Molecular Recognition
- Vol. 1 (2) , 75-79
- https://doi.org/10.1002/jmr.300010205
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Nonpeptide mimetics of .beta.-turns: a facile oxidative intramolecular cycloaddition of an azodicarbonyl systemJournal of the American Chemical Society, 1988
- Methodology for the synthesis of mimetics of peptide β-turnsTetrahedron Letters, 1987
- The Design and Synthesis of a Nonpeptide Mimic of ErabutoxinHETEROCYCLES, 1987
- Correlation between sites of limited proteolysis and segmental mobility in thermolysinBiochemistry, 1986
- The design and synthesis of a nonpeptide mimic of an immunosuppressing peptideTetrahedron Letters, 1986
- 2,8-Dimethyl-4-(carboxymethyl)-6-(aminomethyl)phenoxathiin S-dioxide: an organic substitute for the .beta.-turn in peptides?Journal of the American Chemical Society, 1986
- The immunodominant site of a synthetic immunogen has a conformational preference in water for a type-II reverse turnNature, 1985
- An efficient synthesis of ethyl LL-3-amino-2-piperidone-6-carboxylateThe Journal of Organic Chemistry, 1984
- The role of the hydroxy amino acid in the triplet sequence Asn-Xaa-Thr(Ser) for the N-glycosylation step during glycoprotein biosynthesisBiochemical Journal, 1981
- Experimental and Theoretical Aspects of Protein FoldingAdvances in Protein Chemistry, 1975