Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0040-4039(99)01976-0
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dc.titleAn enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane
dc.contributor.authorLoh, T.-P.
dc.contributor.authorZhou, J.-R.
dc.contributor.authorLi, X.-R.
dc.date.accessioned2014-06-23T05:31:53Z
dc.date.available2014-06-23T05:31:53Z
dc.date.issued1999-12-24
dc.identifier.citationLoh, T.-P., Zhou, J.-R., Li, X.-R. (1999-12-24). An enantioselective indium-mediated allylation reaction of aldehydes and ketones in dichloromethane. Tetrahedron Letters 40 (52) : 9333-9336. ScholarBank@NUS Repository. https://doi.org/10.1016/S0040-4039(99)01976-0
dc.identifier.issn00404039
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75563
dc.description.abstractAn enantioselective indium-mediated addition reaction of allylic bromides to carbonyl compounds was achieved in dichloromethane in the presence of (-)-cinchonidine. The desired products were obtained in moderate to excellent yields and with up to 75% enantioselectivity.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0040-4039(99)01976-0
dc.sourceScopus
dc.subjectAllylation
dc.subjectCarbonyl
dc.subjectEnantioselectivity
dc.subjectIndium
dc.subjectTrifluoromethyl
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/S0040-4039(99)01976-0
dc.description.sourcetitleTetrahedron Letters
dc.description.volume40
dc.description.issue52
dc.description.page9333-9336
dc.description.codenTELEA
dc.identifier.isiut000084099200041
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