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Chembiochem ; 14(5): 564-7, 2013 Mar 18.
Article in English | MEDLINE | ID: mdl-23483642

ABSTRACT

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.


Subject(s)
Multienzyme Complexes/metabolism , Selenium/chemistry , Amino Acid Sequence , Cysteine/chemistry , Cysteine/metabolism , Iodoacetamide/chemistry , Oxazoles/chemistry , Oxazoles/metabolism , Peptides, Cyclic/biosynthesis , Peptides, Cyclic/chemistry , Selenium/metabolism , Selenocysteine/chemistry , Selenocysteine/metabolism , Serine/chemistry , Serine/metabolism , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Thiazoles/chemistry , Thiazoles/metabolism , Threonine/chemistry , Threonine/metabolism
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