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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9380
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:41Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:41Z-
dc.date.issued2014-
dc.identifier.citationBehera, T. K., Nurul Islam, S., Mobin, S. M., & Singh, V. (2014). Cycloaddition of cyclohexa-2,4-dienones with β-nitroacrylates: A short and efficient entry into bicyclo[2.2.2]octanes endowed with β-nitro-ester and β-amino ester functionality. Tetrahedron Letters, 55(37), 5170-5173. doi:10.1016/j.tetlet.2014.07.097en_US
dc.identifier.issn0040-4039-
dc.identifier.otherEID(2-s2.0-84908378577)-
dc.identifier.urihttps://doi.org/10.1016/j.tetlet.2014.07.097-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9380-
dc.description.abstractRegio- and stereoselective cycloaddition of β-nitroacrylates with electron deficient cyclohexa-2,4-dienones leading to highly functionalised bicyclo[2.2.2]octanes having the β-nitroester group and their transformation to bicyclo[2.2.2]octanes having β-aminoester functionality is described. © 2014 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.sourceTetrahedron Lettersen_US
dc.subjectacrylic acid derivativeen_US
dc.subjectalkadieneen_US
dc.subjectbeta amino esteren_US
dc.subjectbeta nitro esteren_US
dc.subjectbeta nitroacrylate derivativeen_US
dc.subjectbicyclo[2.2.2]octane derivativeen_US
dc.subjectcyclohexa 2,4 dienone derivativeen_US
dc.subjectester derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectabsorptionen_US
dc.subjectArticleen_US
dc.subjectcycloadditionen_US
dc.subjectDiels Alder reactionen_US
dc.subjectstereochemistryen_US
dc.subjectstereoisomerismen_US
dc.subjectAlnusen_US
dc.titleCycloaddition of cyclohexa-2,4-dienones with β-nitroacrylates: A short and efficient entry into bicyclo[2.2.2]octanes endowed with β-nitro-ester and β-amino ester functionalityen_US
dc.typeJournal Articleen_US
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