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Enantiopure hydroxymethylated cycloalkenols as privileged small molecular multifunctional scaffolds for the asymmetric synthesis of carbocycles
dc.contributor.authorKumar, R
dc.contributor.authorRej, RK
dc.contributor.authorHalder, J
dc.contributor.authorMandal, H
dc.contributor.authorNanda, S
dc.date.accessioned2023-09-13T13:09:15Z
dc.date.available2023-09-13T13:09:15Z
dc.date.issued2016-07-01
dc.identifier.issn0957-4166
dc.identifier.issn1362-511X
dc.identifier.urihttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000377834700010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=cc40378bfc9614a14500fbd6db90869f
dc.identifier.urihttps://hdl.handle.net/2027.42/177664en
dc.description.abstractEnantiopure hydroxymethylated cycloalkenols bearing a quaternary stereocenter have been synthesized by a Pybox mediated enantioselective desymmetrization method. The synthesized cycloalkenols serve as starting precursors for the construction of several chiral small ring carbocyclic frameworks by a distinct functional group transformation.
dc.languageen
dc.publisherElsevier
dc.titleEnantiopure hydroxymethylated cycloalkenols as privileged small molecular multifunctional scaffolds for the asymmetric synthesis of carbocycles
dc.typeArticle
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/177664/2/Enantiopure hydroxymethylated cycloalkenols.pdf
dc.identifier.doi10.1016/j.tetasy.2016.05.003
dc.identifier.doihttps://dx.doi.org/10.7302/8121
dc.identifier.sourceTetrahedron Asymmetry
dc.description.versionPublished version
dc.date.updated2023-09-13T13:09:14Z
dc.identifier.orcid0000-0003-0904-9137
dc.identifier.volume27
dc.identifier.issue11-12
dc.identifier.startpage498
dc.identifier.endpage512
dc.identifier.name-orcidKumar, R
dc.identifier.name-orcidRej, RK; 0000-0003-0904-9137
dc.identifier.name-orcidHalder, J
dc.identifier.name-orcidMandal, H
dc.identifier.name-orcidNanda, S
dc.working.doi10.7302/8121en
dc.owningcollnameInternal Medicine, Department of


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