Derivatization of Chiral Amines with (S,S)-N-Trifluoroacetylproline Anhydride for GC Estimation of Enantiomeric Composition
- 1 June 1982
- journal article
- research article
- Published by Elsevier in Journal of Pharmaceutical Sciences
- Vol. 71 (6) , 658-661
- https://doi.org/10.1002/jps.2600710613
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Solid-state NMR spectroscopy. Distinction of diastereomers and determination of optical purityJournal of the American Chemical Society, 1979
- Stereochemical aspects of the Pummerer reaction. Regioselectivity as a criterion for the differentiation of ylide and E2 pathways in the product-determining step of the reactions of benzyl methyl halo- and oxysulfonium cationsCanadian Journal of Chemistry, 1979
- In vitro stereoselective metabolism of the psychotomimetic amine, 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane. An apparent enantiomeric interactionJournal of Medicinal Chemistry, 1977
- Synthesis of N-Pentafluorobenzoyl-S-(—)-prolyl 1-Imidazolide, A New Electron-Capture Sensitive Reagent for Determination of Enantiomeric CompositionJournal of Pharmaceutical Sciences, 1973
- 715. Amino-acids and peptides. Part XIX. The mechanism of racemisation during peptide synthesis. “The chloride effect”Journal of the Chemical Society, 1964
- Amino Acid Active Esters. III. Base-Catalyzed Racemization of Peptide Active Esters1,2The Journal of Organic Chemistry, 1962
- N ‐Trifluoracetyl‐aminosäuren, X. N ‐Trifluoracetyl‐ L ‐Asparaginsäure‐Anhydrid und N ‐Trifluoracetyl‐ L ‐Prolin‐AnhydridEuropean Journal of Inorganic Chemistry, 1957