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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19086
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dc.contributor.authorKumar, Indresh-
dc.date.accessioned2025-07-25T06:27:32Z-
dc.date.available2025-07-25T06:27:32Z-
dc.date.issued2025-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2025/ob/d4ob02028f-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19086-
dc.description.abstract2,2-Disubstituted indolin-3-ones, which are essential components in many manufactured chemicals, dyes, and naturally occurring bioactive alkaloids, have emerged as exciting synthetic targets. Much attention has been paid to accessing these units, particularly in an asymmetric fashion, during the last decade. In this review article, we discuss the current state of available methods with existing mechanistic pathways for accessing chiral indolin-3-one derivatives under various catalytic systems. This overall presentation of asymmetric catalytic protocols to access 2,2-disubstituted or fused indolin-3-ones with an aza-quaternary centre is categorized based on the reaction modes of 2-substituted-3H-indole-3-one derivatives or other similar protocols.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectAsymmetric synthesisen_US
dc.subjectAza-quaternary centeren_US
dc.subjectCatalytic asymmetric protocolsen_US
dc.subjectSynthetic methodologiesen_US
dc.subjectDyes and chemical intermediatesen_US
dc.titleRecent developments in the catalytic asymmetric synthesis of indolin-3-one derivativesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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