A new method for the preparation of active esters of various amino acids by oxidation-reduction condensation
- 1 January 1970
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 11 (60) , 5293-5296
- https://doi.org/10.1016/s0040-4039(00)99997-0
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Peptide synthesis via the oxidation-reduction condensation by the use of 2,2′-dipyridyldisulfide as an oxidantTetrahedron Letters, 1970
- A new method for peptide synthesis by oxidation-reduction condensationJournal of the American Chemical Society, 1968
- Pentachlorophenyl esters of N-carbobenzoxy-L-amino acidsThe Journal of Organic Chemistry, 1967
- Synthesis of N-Hydroxysuccinimide Esters of Acyl Peptides by the Mixed Anhydride MethodJournal of the American Chemical Society, 1967
- Über aktivierte Ester, VII. Untersuchungen über die peptidchemische Verwendbarkeit von Acylaminosäure‐chinolyl‐(8)‐esternEuropean Journal of Inorganic Chemistry, 1966
- Umsetzung von Alkalimetallphosphiden mit Salzen aromatischer Sulfonsäuren 2. Mitt.: Die Reaktion substituierter aromatischer Sulfonate mit KaliumdiphenylphosphidMonatshefte für Chemie / Chemical Monthly, 1965
- Die Aktivierung von Acylaminosäuren und Acylpeptiden mit DicyclohexylcarbodiimidEuropean Journal of Organic Chemistry, 1965
- The Use of Esters of N-Hydroxysuccinimide in Peptide SynthesisJournal of the American Chemical Society, 1964
- 163. Amino-acids and peptides. Part XVI. Further studies of racemisation during peptide synthesisJournal of the Chemical Society, 1963
- Synthesis of β-Cyano-L-alanine and γ-Cyano-α-L-aminobutyric Acid, Dehydration Products of L-Asparagine and L-Glutamine; a New Synthesis of Amino Acid NitrilesThe Journal of Organic Chemistry, 1961