Stereoselective routes towards the synthesis of unusual bis(amino acids) and cyclic amino acids
SummaryStereoselective syntheses are described of bridged bis(glycines) as conformationally constrained substitutes for cystine, and of cyclic α-amino acids where the α-carbon of the amino acid is part of a five-, six- or seven-membered ring which may hold a hydroxy group as a threonine analogue.
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| Veröffentlicht in: | International journal of peptide research and therapeutics 1998-05, Vol.5 (2-3), p.227-233 |
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| Format: | Artikel |
| Sprache: | eng |
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| Online-Zugang: | Volltext |
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| Zusammenfassung: | SummaryStereoselective syntheses are described of bridged bis(glycines) as conformationally constrained substitutes for cystine, and of cyclic α-amino acids where the α-carbon of the amino acid is part of a five-, six- or seven-membered ring which may hold a hydroxy group as a threonine analogue. |
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| ISSN: | 0929-5666 1573-3149 1573-496X 1573-3904 |
| DOI: | 10.1007/BF02443474 |