Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2934
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dc.contributor.authorReddy, C.-
dc.contributor.authorBabu, S.A.-
dc.contributor.authorAslam, N.A.-
dc.contributor.authorRajkumar, V.-
dc.date.accessioned2020-12-10T06:29:11Z-
dc.date.available2020-12-10T06:29:11Z-
dc.date.issued2013-
dc.identifier.citationEuropean Journal of Organic Chemistry, 2013(12), pp.2362-2380.en_US
dc.identifier.issnhttps://doi.org/10.1002/ejoc.201201382-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201201382-
dc.identifier.urihttp://hdl.handle.net/123456789/2934-
dc.description.abstractThe indium‐mediated installation of a stereoarray that consists of contiguous tertiary carbinol and all‐carbon stereocenters in functionalized carbocyclic building blocks and bicyclic lactones is presented. The absolute stereochemistry of the products was established for the highly diastereofacial selective addition of allyl and propargyl indiums to α‐alkyl‐α‐(ethoxycarbonyl)cycloalkanones.en_US
dc.language.isoenen_US
dc.publisherWILEY‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.subjectCarbocyclesen_US
dc.subjectDia­stereoselectivityen_US
dc.subjectAllylationen_US
dc.subjectIndiumen_US
dc.titleConstruction of Functionalized Carbocycles Having Contiguous Tertiary Carbinol and All‐Carbon Stereogenic Centersen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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