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|Title:||Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity|
|Authors:||Li, A. |
|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|
|Appears in Collections:||Staff Publications|
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