Please use this identifier to cite or link to this item:
https://doi.org/10.1039/c3cc46675b
DC Field | Value | |
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dc.title | Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity | |
dc.contributor.author | Li, A. | |
dc.contributor.author | Liu, J. | |
dc.contributor.author | Pham, S.Q. | |
dc.contributor.author | Li, Z. | |
dc.date.accessioned | 2014-06-17T07:40:08Z | |
dc.date.available | 2014-06-17T07:40:08Z | |
dc.date.issued | 2013-12-21 | |
dc.identifier.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 | |
dc.identifier.issn | 13597345 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/63836 | |
dc.description.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. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c3cc46675b | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMICAL & BIOMOLECULAR ENGINEERING | |
dc.description.doi | 10.1039/c3cc46675b | |
dc.description.sourcetitle | Chemical Communications | |
dc.description.volume | 49 | |
dc.description.issue | 98 | |
dc.description.page | 11572-11574 | |
dc.description.coden | CHCOF | |
dc.identifier.isiut | 000327260100034 | |
Appears in Collections: | Staff Publications |
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