Chiral secondary amino acids, their importance, and methods of analysis
Author:
Funder
Interreg
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,Clinical Biochemistry,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s00726-022-03136-6.pdf
Reference290 articles.
1. Abe I, Nakahara T (1996) Enantiomer separation of amino acids as their N-alkyloxycarbonyl alkylamide derivatives by chiral phase capillary GC. HRCJ High Resol Chromatogr 19(9):511–514
2. Abe I, Kawazuma M, Fujimoto N, Nakahara T (1995) N-alkyloxycarbonyl isobutylamides as readily prepared diamide derivatives of amino-acids for separation of enantiomeric isomers by chiral phase capillary gas-chromatography. Chem Lett 4:329–330. https://doi.org/10.1246/cl.1995.329
3. Abe I, Minami H, Nakao Y, Nakahara T (2002) N-pivaloyl methyl ester derivatives of amino acids for separation of enantiomers by chiral-phase capillary gas chromatography. J Sep Sci 25(10–11):661–664. https://doi.org/10.1002/1615-9314(20020701)25:10/11%3c661::aid-jssc661%3e3.0.co;2-x
4. Aher RD, Sudalai A (2016) Proline catalyzed enantioselective synthesis of (2S,3S)-3-hydroxypipecolic acid and formal synthesis of (+)-swainsonine. Tetrahedron Lett 57(19):2021–2024. https://doi.org/10.1016/j.tetlet.2016.03.042
5. Aiello A, Fattorusso E, Giordano A, Menna M, Muller WEG, Perovic-Ottstadt S, Schroder HC (2007) Damipipecolin and damituricin, novel bioactive bromopyrrole alkaloids from the Mediterranean sponge Axinella damicornis. Bioorg Med Chem 15(17):5877–5887. https://doi.org/10.1016/j.bmc.2007.05.074
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