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Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9408
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dc.contributor.authorBiswas, Soumenen_US
dc.contributor.authorMobin, Shaikh M.en_US
dc.contributor.authorSamanta, Sampaken_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:32:52Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:32:52Z-
dc.date.issued2013-
dc.identifier.citationBiswas, S., Jaiswal, P. K., Singh, S., Mobin, S. M., & Samanta, S. (2013). L-proline catalyzed stereoselective synthesis of (E)-methyl-α-indol- 2-yl-β-aryl/alkyl acrylates: Easy access to substituted carbazoles, γ-carbolines and prenostodione. Organic and Biomolecular Chemistry, 11(41), 7084-7087. doi:10.1039/c3ob41573ben_US
dc.identifier.issn1477-0520-
dc.identifier.otherEID(2-s2.0-84885145979)-
dc.identifier.urihttps://doi.org/10.1039/c3ob41573b-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9408-
dc.description.abstractA simple, mild and robust method for the stereoselective synthesis of (E)-methyl α-(3-formyl-1H-indol-2-yl)-β-aryl/alkyl-substituted acrylates via a condensation reaction of methyl 2-(3-formyl-1H-indol-2-yl) acetate with several alkyl or aryl aldehydes using l-proline (25 mol%) as a catalyst is presented for the first time. In addition, completely metal free based high yielding methods for the syntheses of highly substituted biologically important carbazoles, γ-carbolines and the marine alkaloid prenostodione have been developed through our methodology. © 2013 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.sourceOrganic and Biomolecular Chemistryen_US
dc.subjectAryl aldehydesen_US
dc.subjectCarbolinesen_US
dc.subjectL-prolineen_US
dc.subjectMarine alkaloidsen_US
dc.subjectMetal freeen_US
dc.subjectRobust methodsen_US
dc.subjectStereoselective synthesisen_US
dc.subjectCondensation reactionsen_US
dc.subjectPolycyclic aromatic hydrocarbonsen_US
dc.subjectPyridineen_US
dc.subjectSaltsen_US
dc.subjectStereochemistryen_US
dc.subjectStereoselectivityen_US
dc.subjectacrylic acid derivativeen_US
dc.subjectcarbazole derivativeen_US
dc.subjectcarboline derivativeen_US
dc.subjectgamma carbolineen_US
dc.subjectgamma-carbolineen_US
dc.subjectindole derivativeen_US
dc.subjectprenostodioneen_US
dc.subjectprolineen_US
dc.subjectarticleen_US
dc.subjectcatalysisen_US
dc.subjectchemical structureen_US
dc.subjectchemistryen_US
dc.subjectstereoisomerismen_US
dc.subjectsynthesisen_US
dc.subjectAcrylatesen_US
dc.subjectCarbazolesen_US
dc.subjectCarbolinesen_US
dc.subjectCatalysisen_US
dc.subjectIndolesen_US
dc.subjectMolecular Structureen_US
dc.subjectProlineen_US
dc.subjectStereoisomerismen_US
dc.titleL-Proline catalyzed stereoselective synthesis of (E)-methyl-α-indol- 2-yl-β-aryl/alkyl acrylates: Easy access to substituted carbazoles, γ-carbolines and prenostodioneen_US
dc.typeJournal Articleen_US
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