Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/75436
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dc.titleA highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water
dc.contributor.authorLoh, T.-P.
dc.contributor.authorLi, X.-R.
dc.date.accessioned2014-06-23T05:30:20Z
dc.date.available2014-06-23T05:30:20Z
dc.date.issued1997
dc.identifier.citationLoh, T.-P.,Li, X.-R. (1997). A highly stereoselective synthesis of β-trifluoromethylated homoallylic alcohols in water. Angewandte Chemie - International Edition in English 36 (9) : 980-982. ScholarBank@NUS Repository.
dc.identifier.issn05700833
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75436
dc.description.abstractA tin-mediated, indium trichloride promoted allylation reaction provided β-trifluoromethylated homoallylic alcohols, the building blocks of biologically active substances, in high yields and excellent stereoselectivity. Since the syntheses can be carried out in water, the reactive OH groups do not need to be protected, and even compounds that are insoluble in organic solvents can be used.
dc.sourceScopus
dc.subjectaldehydes
dc.subjectallylation
dc.subjectfluorine
dc.subjectindium
dc.subjecttin
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.sourcetitleAngewandte Chemie - International Edition in English
dc.description.volume36
dc.description.issue9
dc.description.page980-982
dc.description.codenACIEA
dc.identifier.isiutNOT_IN_WOS
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