Synthesis of (ϵ‐ 13 C‐,ϵ‐ 15 N)‐Enriched L ‐Lysine − Establishing Schemes for the Preparation of All Possible 13 C and 15 N Isotopomers of L ‐Lysine, L ‐Ornithine, and L ‐Proline
In this paper we describe a simple synthetic strategy that, with the right rational adaptation, gives direct access to any 13 C/ 15 N isotopomer of L ‐glutamate, L ‐ornithine, L ‐proline, L ‐lysine, and L ‐α amino adipic acid. This strategy also allows access to nonproteinogenic amino acids like L ‐...
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Veröffentlicht in: | European journal of organic chemistry 2004-11, Vol.2004 (21), p.4391-4396 |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In this paper we describe a simple synthetic strategy that, with the right rational adaptation, gives direct access to any
13
C/
15
N isotopomer of
L
‐glutamate,
L
‐ornithine,
L
‐proline,
L
‐lysine, and
L
‐α amino adipic acid. This strategy also allows access to nonproteinogenic amino acids like
L
‐citrulline in high yields and optical purity. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) |
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ISSN: | 1434-193X 1099-0690 |
DOI: | 10.1002/ejoc.200400370 |