Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol048608q
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dc.titleHighly efficient chemical kinetic resolution of bishomoallylic alcohols: Synthesis of (R)-sulcatol
dc.contributor.authorChen, S.-L.
dc.contributor.authorHu, Q.-Y.
dc.contributor.authorLoh, T.-P.
dc.date.accessioned2014-10-16T08:30:11Z
dc.date.available2014-10-16T08:30:11Z
dc.date.issued2004-09-16
dc.identifier.citationChen, S.-L., Hu, Q.-Y., Loh, T.-P. (2004-09-16). Highly efficient chemical kinetic resolution of bishomoallylic alcohols: Synthesis of (R)-sulcatol. Organic Letters 6 (19) : 3365-3367. ScholarBank@NUS Repository. https://doi.org/10.1021/ol048608q
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93937
dc.description.abstract(Chemical Equation Presented) A highly efficient chemical kinetic resolution of bishomoallylic alcohols was developed when the alcohols underwent In(OTf)3-catalyzed 3,5-oxonium-ene-type cyclization with steroidal aldehyde 2. Consistently high enantiomeric excess (up to >99%) was obtained.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol048608q
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol048608q
dc.description.sourcetitleOrganic Letters
dc.description.volume6
dc.description.issue19
dc.description.page3365-3367
dc.identifier.isiut000223794600038
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