A Proposal for Using Mild Bases in the Preparation of Optically Pure Peptides
- 1 March 1967
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 40 (3), 656-661
- https://doi.org/10.1246/bcsj.40.656
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- t-Amyloxycarbonyl as a New Protecting Group in Peptide Synthesis. III. An Unexpected Side-reaction during the Synthesis of t-Amyloxycarbonylamino AcidsBulletin of the Chemical Society of Japan, 1967
- Racemization Control in the Synthesis of Peptides by the Mixed Carbonic-Carboxylic Anhydride MethodJournal of the American Chemical Society, 1966
- Optically Active Peptide Oxazolones. Preliminary Racemization Studies under Peptide-Coupling ConditionsJournal of the American Chemical Society, 1965
- The Use of Esters of N-Hydroxysuccinimide in Peptide SynthesisJournal of the American Chemical Society, 1964
- 8-L-Citrulline Vasopressin and 8-L-Citrulline OxytocinJournal of the American Chemical Society, 1962
- N,N'-Carbonyldiimidazole, a New Peptide Forming Reagent1Journal of the American Chemical Society, 1960
- Synthesis of a Biologically Active Analog of Oxytocin, with Phenylalanine Replacing Tyrosine1,2Journal of the American Chemical Society, 1959
- RACEMIZATION BY THE DICYCLOHEXYLCARBODIIMIDE METHOD OF PEPTIDE SYNTHESISJournal of the American Chemical Society, 1958
- Use of Apparent Dissociation Constants in Qualitative Organic AnalysisAnalytical Chemistry, 1954
- Preliminary Investigations on the Preparation of Optically Active Peptides Using Mixed Carbonic—Carboxylic Acid AnhydridesJournal of the American Chemical Society, 1952