Corey L Jones, Alandra Quinn, Xiaochun Alex Wang, Jason K. Smith, Jeffrey Casavant, Simon Berritt, Thomas Knauber, Carlos Martinez, Jovan Livada, Scott P. France, Paul Richardson, Roger Howard, Hatice Gizem Yayla
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Photoenzymatically-Induced Asymmetric Hydroarylation of Alkenes with (Hetero)aryl Halides
A set of stereocomplementary ene-reductase enzymes are described which, when induced by light and aided by an exogenous photocatalyst, catalyze the coupling of (hetero)aryl halides and alkenes in an asymmetric intermolecular hydroarylation process. Thus, carbon scaffolds containing C(sp2)-C(sp3) bonds are synthesized enzymatically from simple precursors in excellent enantiomeric excess. Furthermore, an intramolecular mode is presented with improved yield.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.