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dc.contributor.authorWu, Tung-Kungen_US
dc.contributor.authorChang, Cheng-Hsiangen_US
dc.contributor.authorWen, Hao-Yuen_US
dc.contributor.authorLiu, Yuan-Tingen_US
dc.contributor.authorLi, Wen-Hsuanen_US
dc.contributor.authorWang, Tsai-Tingen_US
dc.contributor.authorShie, Wen-Shiangen_US
dc.date.accessioned2014-12-08T15:07:25Z-
dc.date.available2014-12-08T15:07:25Z-
dc.date.issued2010-02-05en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol902694yen_US
dc.identifier.urihttp://hdl.handle.net/11536/5850-
dc.description.abstractThe Saccharomyces cerevisiae ERG7(Phe699) mutants produced one chair-chair-chair (C-C-C) and two chair-boat-chair (C-B-C) truncated tricyclic compounds, one tetracyclic 17 alpha-exocyclic unrearranged intermediate, and two 17 beta-exocyclic truncated rearranged intermediates. These results provided direct evidence for the importance of the residue in affecting mechanistic transitions between C-B-C and C-C-C substrate conformation and between the 17 alpha- and 17 beta-exocyclic side chain stereochemistry as well as in stabilizing the 6 -6-5 tricyclic and the protosteryl C-17 cations.en_US
dc.language.isoen_USen_US
dc.titleAlteration of the Substrate's Prefolded Conformation and Cyclization Stereochemistry of Oxidosqualene-Lanosterol Cyclase of Saccharomyces cerevisiae by Substitution at Phenylalanine 699en_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol902694yen_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume12en_US
dc.citation.issue3en_US
dc.citation.spage500en_US
dc.citation.epage503en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000273982600026-
dc.citation.woscount9-
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