Please use this identifier to cite or link to this item: http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/564
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dc.contributor.authorVanlaldinpuia, K-
dc.date.accessioned2024-06-12T05:29:04Z-
dc.date.available2024-06-12T05:29:04Z-
dc.date.issued2023-10-23-
dc.identifier.urihttp://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/564-
dc.description.abstractThe preparation of a new class of six bifunctional thiourea organocatalysts having a Dfructose scaffold and a primary amino group was demonstrated. In the present study, the novel organocatalysts exhibited excellent enantio- and moderate diastereoselectivities in the asymmetric Michael addition of aliphatic ketones and 1,3-diketone to substituted nitroolefins at room temperature. In addition, the direct asymmetric aldol reaction between cyclic aliphatic ketone and aromatic aldehydes was also studied in the presence of the saccharide-thiourea organocatalysts giving excellent yield with moderate enantioselectivity.en_US
dc.language.isoen_USen_US
dc.subjectcarbohydrates; bifunctional thiourea; organocatalyst; enantioselective; Michael addition; aldol reactionen_US
dc.titleSynthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactionsen_US
dc.typeOtheren_US
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