Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/71439
DC FieldValueLanguage
dc.contributor.authorWang, Y.C.en_US
dc.contributor.authorHwang, J.Y.en_US
dc.contributor.authorChen, Y.C.en_US
dc.contributor.authorChuang, S.C.en_US
dc.contributor.authorYan, T.H.en_US
dc.date2000zh_TW
dc.date.accessioned2014-06-11T06:01:31Z-
dc.date.available2014-06-11T06:01:31Z-
dc.identifier.issn0957-4166zh_TW
dc.identifier.urihttp://hdl.handle.net/11455/71439-
dc.description.abstractOne-pot deacylation-debromination reactions involving the transesterification of the initial chiral beta-bromo-beta-hydroxy thioimide aldol adducts and subsequent Al-Hg mediated reductive cleavage of the C-Br bond allow for a facile synthesis of enantiopure beta-hydroxy esters. (C) 2000 Published by Elsevier Science Ltd.en_US
dc.language.isoen_USzh_TW
dc.relationTetrahedron-Asymmetryen_US
dc.relation.ispartofseriesTetrahedron-Asymmetry, Volume 11, Issue 8, Page(s) 1797-1800.en_US
dc.relation.urihttp://dx.doi.org/10.1016/s0957-4166(00)00109-9en_US
dc.subjectasymmetric aldol reactionen_US
dc.subjectsilyl ketene acetalsen_US
dc.subjectachiral aldehydesen_US
dc.subjectenolateen_US
dc.titleA facile method for the synthesis of enantiopure alpha-unsubstituted beta-hydroxy estersen_US
dc.typeJournal Articlezh_TW
dc.identifier.doi10.1016/s0957-4166(00)00109-9zh_TW
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.fulltextno fulltext-
item.languageiso639-1en_US-
item.grantfulltextnone-
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