Zinc-Mediated Allylation Followed by Lactonization of Dialkyl 2-(3-Oxo-1,3-diarylpropyl)malonates: Construction of δ-Lactones with Multiple Stereocenters

dc.contributor.authorReddy, C.
dc.contributor.authorBabu, S.A.
dc.date.accessioned2020-12-08T05:12:31Z
dc.date.available2020-12-08T05:12:31Z
dc.date.issued2015
dc.description.abstractA variety of polysubstituted δ-lactones containing three or four stereocenters were prepared from various dialkyl 2-(3-oxo-1,3-diarylpropyl)malonates by a Barbier-type zinc-mediated allylation or cyclohexenylation of the keto group, followed by intramolecular lactonization/transesterification. The stereochemistry of the major isomers was confirmed by X-ray crystal structure analysis of representative compoundsen_US
dc.identifier.citationSynlett, 26(15)en_US
dc.identifier.other10.1055/s-0035-1560052
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560052
dc.identifier.urihttp://hdl.handle.net/123456789/2781
dc.language.isoen_USen_US
dc.publisherGeorg Thieme Verlagen_US
dc.subjectallylationen_US
dc.subjectdiastereoselectivityen_US
dc.subjectlactonesen_US
dc.subjectstereoselective synthesisen_US
dc.titleZinc-Mediated Allylation Followed by Lactonization of Dialkyl 2-(3-Oxo-1,3-diarylpropyl)malonates: Construction of δ-Lactones with Multiple Stereocentersen_US
dc.typeArticleen_US

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