Racemization during aminolysis of mixed and symmetrical anhydrides of N‐alkoxycarbonylamino acids by amino acid anions in aqueous dimethylformamide
- 1 May 1988
- journal article
- Published by Wiley in International Journal of Peptide and Protein Research
- Vol. 31 (5), 443-446
- https://doi.org/10.1111/j.1399-3011.1988.tb00901.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Activation and racemization in peptide bond formationPublished by Springer Nature ,1988
- Mixed anhydrides in peptide synthesis. A study of urethane formation with a contribution on minimization of racemizationCanadian Journal of Chemistry, 1987
- The preparation and reactions of mixed anhydrides of N-alkoxycarbonylamino acidsCanadian Journal of Chemistry, 1987
- The crystal structure of N,N′-bismethoxycarbonyl-L-valyl-L-valine, a product of the rearrangement of the symmetrical anhydride of N-methoxycarbonyl-L-valineCanadian Journal of Chemistry, 1986
- General procedure for preparing a reference mixture and determining the amount of dipeptide contaminant in N‐alkoxycarbonylamino acids by high‐performance liquid chromatographyInternational Journal of Peptide and Protein Research, 1986
- The relative susceptibility to racemization of L- and D-residues in peptide synthesisTetrahedron Letters, 1981
- Enhancement of peptide coupling reactions by 4‐dimethylaminopyridineInternational Journal of Peptide and Protein Research, 1981
- Peptide synthesis in partially aqueous solutionFEBS Letters, 1981
- 2-Alkoxy-5(4H)-oxazolones from N-alkoxycarbonylamino acids and their implication in carbodiimide-mediated reactions in peptide synthesisCanadian Journal of Chemistry, 1981
- Not the alkoxycarbonylamino-acid O-acylisoureaJournal of the Chemical Society, Chemical Communications, 1981