Please use this identifier to cite or link to this item:
|Title:||Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity|
|Authors:||Li, A. |
|Source:||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|
Show full item record
Files in This Item:
There are no files associated with this item.
checked on Mar 7, 2018
WEB OF SCIENCETM
checked on Jan 31, 2018
checked on Mar 11, 2018
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.