Nicotinamide-independent asymmetric bioreduction of C 000000000000 000000000000 000000000000 111111111111 000000000000 111111111111 000000000000 000000000000 000000000000 C-bonds via disproportionation of enones catalyzed by enoate reductases

Autor: Stueckler, Clemens, Reiter, Tamara C., Baudendistel, Nina, Faber, Kurt
Jazyk: angličtina
Rok vydání: 2010
Předmět:
Zdroj: Tetrahedron
ISSN: 0040-4020
Popis: The asymmetric bioreduction of activated CC-bonds catalyzed by a single flavoprotein was achieved via direct hydrogen transfer from a sacrificial 2-enone or 1,4-dione as hydrogen donor without requirement of a nicotinamide cofactor. Due to its simplicity, this system has clear advantages over conventional FAD-recycling systems.
Graphical abstract
Databáze: OpenAIRE