4.4 Article

An Enzymatic Route to Selenazolines

期刊

CHEMBIOCHEM
卷 14, 期 5, 页码 564-567

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201300037

关键词

biochemistry; biosynthesis; patellamides; selenazolines

资金

  1. Leverhulme Trust [RPG-2012-504]
  2. Wellcome Trust [086036]
  3. BBSRC [BB/H001212/1, BB/K015508/1, BB/H005447/1] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/K015508/1, BB/H005447/1, BB/H001212/1, 1098674] Funding Source: researchfish

向作者/读者索取更多资源

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.

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