1. IDR@IIT Indore
  2. IITI Scholarly Publications
  3. Department of Chemistry
Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9133
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMajumdar, Bijuen_US
dc.contributor.authorMandani, Sonamen_US
dc.contributor.authorBhattacharya, Tamalikaen_US
dc.contributor.authorSarma, Daisyen_US
dc.contributor.authorSarma, Tridib Kumaren_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:31:13Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:31:13Z-
dc.date.issued2017-
dc.identifier.citationMajumdar, B., Mandani, S., Bhattacharya, T., Sarma, D., & Sarma, T. K. (2017). Probing carbocatalytic activity of carbon nanodots for the synthesis of biologically active Dihydro/Spiro/Glyco quinazolinones and aza-michael adducts. Journal of Organic Chemistry, 82(4), 2097-2106. doi:10.1021/acs.joc.6b02914en_US
dc.identifier.issn0022-3263-
dc.identifier.otherEID(2-s2.0-85013187610)-
dc.identifier.urihttps://doi.org/10.1021/acs.joc.6b02914-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/9133-
dc.description.abstractHerein, we report the fluorescent carbon dots as an effective and recyclable carbocatalyst for the generation of carbon-heteroatom bond leading to quinazolinone derivatives and aza-Michael adducts under mild reaction conditions. The results establish this nanoscale form of carbon as an alternative carbocatalyst for important acid catalyzed organic transformations. The mild surface acidity of carbon dots imparted by -COOH functionality could effectively catalyze the formation of synthetically challenging spiro/glycoquinazolinones under the present reaction conditions. © 2017 American Chemical Society.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceJournal of Organic Chemistryen_US
dc.subjectAddition reactionsen_US
dc.subjectCarbon nanodotsen_US
dc.subjectCarbon-heteroatom bondsen_US
dc.subjectMichael adductsen_US
dc.subjectMild reaction conditionsen_US
dc.subjectOrganic transformationsen_US
dc.subjectQuinazolinonesen_US
dc.subjectReaction conditionsen_US
dc.subjectSurface acidityen_US
dc.subjectChemical reactionsen_US
dc.subjectcarbonen_US
dc.subjectcarbon nanodoten_US
dc.subjectcarbon nanoparticleen_US
dc.subjectcarboxylic aciden_US
dc.subjectdihydroquinazolinone derivativeen_US
dc.subjectfunctional groupen_US
dc.subjectglycoquinazolinone derivativeen_US
dc.subjectquinazolinone derivativeen_US
dc.subjectspiroquinazolinone derivativeen_US
dc.subjectunclassified drugen_US
dc.subjectcarbon nanotubeen_US
dc.subjectfluorescent dyeen_US
dc.subjectheterocyclic compounden_US
dc.subjectquinazolinone derivativeen_US
dc.subjectacidityen_US
dc.subjectArticleen_US
dc.subjectaza Michael additionen_US
dc.subjectcatalysisen_US
dc.subjectcatalysten_US
dc.subjectchemical bonden_US
dc.subjectchemical reactionen_US
dc.subjectcyclocondensationen_US
dc.subjectdrug structureen_US
dc.subjectdrug synthesisen_US
dc.subjectMichael additionen_US
dc.subjectsurface propertyen_US
dc.subjectcatalysisen_US
dc.subjectchemical structureen_US
dc.subjectchemistryen_US
dc.subjectsynthesisen_US
dc.subjectAza Compoundsen_US
dc.subjectCatalysisen_US
dc.subjectFluorescent Dyesen_US
dc.subjectMolecular Structureen_US
dc.subjectNanotubes, Carbonen_US
dc.subjectQuinazolinonesen_US
dc.titleProbing Carbocatalytic Activity of Carbon Nanodots for the Synthesis of Biologically Active Dihydro/Spiro/Glyco Quinazolinones and Aza-Michael Adductsen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: