Lotter, JBotes, ALDyk, MSBreytenbach, JC2007-02-062007-06-072007-02-062007-06-072004-08Lotter, J, et al. 2004. Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase. Biotechology Letters, vol 26 (15), pp 1197-12000141-5492http://hdl.handle.net/10204/1515http://hdl.handle.net/10204/1515Kinetic resolution of the enantiomers of trans-1-phenylpropene oxide and (2,3-epoxypropyl)benzene was achieved by yeasts from the genus Rhodotorula. The resolution of trans-1-phenylpropene oxide by Rhodotorula glutinis UOFS Y-0123 yielded (1R, 2R)-epoxide (ee >98%, yield 30%) and (1R, 2S)-diol (ee 95%, yield 40%). The highest enantio- and region selectivity toward (2,3-epoxypropyl)benzene resided in Rhodotorula sp. UOFS Y-0448 (E = 6.16), yielding (S)-epoxide (ee 64%, yield 33%) and (R)-diol (ee 67%, yield 28%). This confirms the superiority of yeasts from the Basidiomycetes genera in the enantio selective hydrolysis of epoxides from different structural classes.127418 bytesapplication/pdfenCopyright: 2004 Kluwer Academic PublisherBiotransformationsEpoxide hydrolasesKinetic resolutionsArticleLotter, J., Botes, A., Dyk, M., & Breytenbach, J. (2004). Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase. http://hdl.handle.net/10204/1515Lotter, J, AL Botes, MS Dyk, and JC Breytenbach "Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase." (2004) http://hdl.handle.net/10204/1515Lotter J, Botes A, Dyk M, Breytenbach J. Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase. 2004; http://hdl.handle.net/10204/1515.TY - Article AU - Lotter, J AU - Botes, AL AU - Dyk, MS AU - Breytenbach, JC AB - Kinetic resolution of the enantiomers of trans-1-phenylpropene oxide and (2,3-epoxypropyl)benzene was achieved by yeasts from the genus Rhodotorula. The resolution of trans-1-phenylpropene oxide by Rhodotorula glutinis UOFS Y-0123 yielded (1R, 2R)-epoxide (ee >98%, yield 30%) and (1R, 2S)-diol (ee 95%, yield 40%). The highest enantio- and region selectivity toward (2,3-epoxypropyl)benzene resided in Rhodotorula sp. UOFS Y-0448 (E = 6.16), yielding (S)-epoxide (ee 64%, yield 33%) and (R)-diol (ee 67%, yield 28%). This confirms the superiority of yeasts from the Basidiomycetes genera in the enantio selective hydrolysis of epoxides from different structural classes. DA - 2004-08 DB - ResearchSpace DP - CSIR KW - Biotransformations KW - Epoxide hydrolases KW - Kinetic resolutions LK - https://researchspace.csir.co.za PY - 2004 SM - 0141-5492 T1 - Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase TI - Hydrolytic kinetic resolution of the enantiomers of the structural isomers trans-1-phenylpropene oxide and (2,3-epoxypropyl) benzene by yeast epoxide hydrolase UR - http://hdl.handle.net/10204/1515 ER -