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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9308
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:13Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:13Z-
dc.date.issued2015-
dc.identifier.citationSingh, V., Das, B., Jarhad, D. B., & Mobin, S. M. (2015). Molecular diversity from aromatics. cycloaddition of cyclohexa-2,4-dienones, ring-closing metathesis and sigmatropic shifts: A general and stereoselective route to novel spirocarbocyclics. Tetrahedron, 71(4), 560-576. doi:10.1016/j.tet.2014.12.033en_US
dc.identifier.issn0040-4020-
dc.identifier.otherEID(2-s2.0-84920494623)-
dc.identifier.urihttps://doi.org/10.1016/j.tet.2014.12.033-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9308-
dc.description.abstractA novel, general and stereoselective route to spiroannulated bicyclo[2.2.2]octenones and their transformation to spiroannulated bicyclo[3.3.0]- and bicyclo[4.2.0]octanes is described. Oxidative dearomatization of o-hydroxymethylphenols, cycloaddition of spiroepoxycyclohexadienones, ring-closing metathesis and photochemical sigmatropic 1,2- and 1,3-acyl shifts are the key features of our methodology. ©2014 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.sourceTetrahedronen_US
dc.subject2 hydroxymethylphenol derivativeen_US
dc.subjectaromatic compounden_US
dc.subjectbicyclo[2.2.2]octane derivativeen_US
dc.subjectbicyclo[2.2.2]octenone derivativeen_US
dc.subjectbicyclo[3.3.0]octane derivativeen_US
dc.subjectbicyclo[4.2.0]octane derivativeen_US
dc.subjectepoxideen_US
dc.subjectphenol derivativeen_US
dc.subjectspiroepoxycyclohexadienone derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectaromatizationen_US
dc.subjectArticleen_US
dc.subjectcycloadditionen_US
dc.subjectoxidationen_US
dc.subjectoxidative dearomatizationen_US
dc.subjectphotochemistryen_US
dc.subjectring closing metathesisen_US
dc.subjectstereochemistryen_US
dc.subjectAlnusen_US
dc.titleMolecular diversity from aromatics. Cycloaddition of cyclohexa-2,4-dienones, ring-closing metathesis and sigmatropic shifts: A general and stereoselective route to novel spirocarbocyclicsen_US
dc.typeJournal Articleen_US
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