Internally stabilized selenocysteine derivatives: syntheses, <SUP>77</SUP>Se NMR and biomimetic studies

Selenocystine ([Sec]<SUB>2</SUB>) 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 (<SUP>1</SUP>H, <SUP>13</SUP>C and <SUP>77</SUP>Se) 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