Please use this identifier to cite or link to this item: https://doi.org/10.1039/c3cc46675b
Title: Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity
Authors: Li, A. 
Liu, J.
Pham, S.Q.
Li, Z. 
Issue Date: 21-Dec-2013
Citation: Li, A., Liu, J., Pham, S.Q., Li, Z. (2013-12-21). Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity. Chemical Communications 49 (98) : 11572-11574. ScholarBank@NUS Repository. https://doi.org/10.1039/c3cc46675b
Abstract: A triple mutant of P450pyr monooxygenase (P450pyrTM) catalysed the epoxidation of several para-substituted styrenes as the first enzyme showing high (R)-enantioselectivity and high conversion, demonstrated a broad substrate range, and showed high enantioselectivity for the epoxidation of an unconjugated 1,1-disubstituted alkene, 2-methyl-3-phenyl-1-propene, and a cyclic alkene, N-phenoxycarbonyl-1,2,5,6-tetrahydropyridine, respectively. © 2013 The Royal Society of Chemistry.
Source Title: Chemical Communications
URI: http://scholarbank.nus.edu.sg/handle/10635/63836
ISSN: 13597345
DOI: 10.1039/c3cc46675b
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