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• W2000579815 abstract "Selenocystine ([Sec]2) and aryl-substituted selenocysteine (Sec) derivatives are synthesized, starting from commercially available amino acid L-serine. These compounds are characterized by a number of analytical techniques such as NMR (1H, 13C and 77Se) and TOF mass spectroscopy. This study reveals that the introduction of amino/imino substituents capable of interacting with selenium may stabilize the Sec derivatives. This study further suggests that the oxidation–elimination reactions in Sec derivatives could be used for the generation of biologically active selenols having internally stabilizing substituents." @default.
• W2000579815 created "2016-06-24" @default.
• W2000579815 creator A5032638949 @default.
• W2000579815 creator A5056827030 @default.
• W2000579815 date "2005-01-01" @default.
• W2000579815 modified "2023-10-12" @default.
• W2000579815 title "Internally stabilized selenocysteine derivatives: syntheses, 77Se NMR and biomimetic studies" @default.
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• W2000579815 doi "https://doi.org/10.1039/b505299h" @default.
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