Here we report on the stereoselective benzylic hydroxylation and C1–C2 epoxidation of alkylbenzenes and styrene derivatives, respectively, by a heme-thiolate peroxygenase (EC 1.11. 2.1) from the fungus Agrocybe aegerita. Benzylic hydroxylation led exclusively to the (R)-1-phenylalkanols. For (R)-1-phenylethanol,(R)-1-phenylpropanol and (R)-1-tetralol, the ee reached> 99%. For longer chain lengths, the enantiomeric excesses (ee) and total ...
[Efange, Simon M. N.; Khare, Anil B.; Von Hohenberg, Krystyna; MacH, Robert H.; Parsons, Stanley M.; Tu, Zhude Journal of Medicinal Chemistry, 2010 , vol. 53, # 7 p. 2825 - 2835]
[Rogers, Gary A.; Parsons, Stanley M.; Anderson, D. C.; Nilsson, Lena M.; Bahr, Ben A.; et al. Journal of Medicinal Chemistry, 1989 , vol. 32, # 6 p. 1217 - 1230]