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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19074
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2025-07-24T07:17:29Z-
dc.date.available2025-07-24T07:17:29Z-
dc.date.issued2024-09-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlehtml/2024/ob/d4ob01168f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19074-
dc.description.abstractA simple and straightforward method has been developed to access distinctly substituted β-(3-indolyl)acroleins and β-(imidazo[1,2-a]pyridin-3-yl)acroleins using propargyl alcohol as an acrolein equivalent. A broad substrate scope, good yields, easily accessible substrates, and metal-free conditions are the salient features of the developed methodology. This work contributes to a significant advancement in the sustainable synthesis of functionalized acroleinsen_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectβ-(3-indolyl)acroleinsen_US
dc.subjectPropargyl alcoholen_US
dc.subjectAcrolein equivalenten_US
dc.subjectSustainable methodologyen_US
dc.subjectHeterocyclic synthesisen_US
dc.titlePropargyl alcohol as an acrolein equivalent: synthesis of β-(3-indolyl)acroleins and β-(imidazo[1,2-a]pyridin-3-yl)acroleinsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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