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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9343
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dc.contributor.authorMobin, Shaikh M.en_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:26Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:26Z-
dc.date.issued2014-
dc.identifier.citationDas, B., Mobin, S. M., & Singh, V. (2014). Studies on synthesis of spirolactone annulated bicyclo[2.2.2]octanes: Tricyclic core of yaoshanenolides. Tetrahedron, 70(32), 4768-4777. doi:10.1016/j.tet.2014.05.043en_US
dc.identifier.issn0040-4020-
dc.identifier.otherEID(2-s2.0-84902248916)-
dc.identifier.urihttps://doi.org/10.1016/j.tet.2014.05.043-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9343-
dc.description.abstractA stereoselective approach to tricyclic core of yaoshanenolides from simple aromatic precursor is described. Cycloaddition of highly reactive spiroepoxycyclohexa-2,4-dienone, stereoselective Grignard reaction, alkylation, and ring-closing metathesis reaction are the key features of our approach. © 2014 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.publisherElsevier Ltden_US
dc.sourceTetrahedronen_US
dc.subjectbicyclo[2.2.2]octane derivativeen_US
dc.subjectspironolactoneen_US
dc.subjectalkylationen_US
dc.subjectarticleen_US
dc.subjectcarbon nuclear magnetic resonanceen_US
dc.subjectcolumn chromatographyen_US
dc.subjectcrystal structureen_US
dc.subjectcycloadditionen_US
dc.subjectdecarboxylationen_US
dc.subjectDiels Alder reactionen_US
dc.subjectGrignard reactionen_US
dc.subjectJones oxidationen_US
dc.subjectnucleophilicityen_US
dc.subjectpriority journalen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectring closing metathesisen_US
dc.subjectstereochemistryen_US
dc.subjectstereoisomerismen_US
dc.subjectsynthesisen_US
dc.subjectthin layer chromatographyen_US
dc.subjectX ray analysisen_US
dc.titleStudies on synthesis of spirolactone annulated bicyclo[2.2.2]octanes: Tricyclic core of yaoshanenolidesen_US
dc.typeJournal Articleen_US
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