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Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/95320
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dc.titleTin- and indium-mediated allylation reactions in water: Highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols
dc.contributor.authorLoh, T.-P.
dc.contributor.authorLi, X.-R.
dc.date.accessioned2014-10-16T08:46:25Z
dc.date.available2014-10-16T08:46:25Z
dc.date.issued1999-08
dc.identifier.citationLoh, T.-P.,Li, X.-R. (1999-08). Tin- and indium-mediated allylation reactions in water: Highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols. European Journal of Organic Chemistry (8) : 1893-1899. ScholarBank@NUS Repository.
dc.identifier.issn1434193X
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/95320
dc.description.abstractThe indium-mediated allylation reaction of aldehydes with 4-bromo- 1,1,1-trifluoro-2-butene in water afforded β-trifluoromethylated homoallylic alcohols in high yields. In most cases, high regio- and excellent diastereoselectivities were obtained.
dc.sourceScopus
dc.subject1,1,1-Trifluoro-4-bromobut-2-ene
dc.subjectAldehydes
dc.subjectAllylation
dc.subjectIndium
dc.subjectTin
dc.subjectWater
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleEuropean Journal of Organic Chemistry
dc.description.issue8
dc.description.page1893-1899
dc.description.codenEJOCF
dc.identifier.isiutNOT_IN_WOS
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