Biomedical Science Research Complex, University of St Andrews, North Haugh, St. Andrews, KY16 9ST, UK.
Chembiochem. 2013 Mar 18;14(5):564-7. doi: 10.1002/cbic.201300037. Epub 2013 Feb 18.
Ringing the changes: Selenazolines have applications in medicinal chemistry, but their synthesis is challenging. We report a new convenient and less toxic route to these heterocycles that starts from commercially available selenocysteine. The new route depends on a heterocyclase enzyme that creates oxazolines and thiazolines from serines/threonines and cysteines.
硒唑啉在药物化学中有应用,但它们的合成颇具挑战性。我们报告了一种新的、毒性更小的合成这些杂环的方法,该方法从商业可得的硒半胱氨酸开始。这条新路线依赖于一种杂环酶,它能将丝氨酸/苏氨酸和半胱氨酸转化为唑啉和噻唑啉。