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Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Vanlaldinpuia, K | - |
dc.date.accessioned | 2024-06-12T05:29:04Z | - |
dc.date.available | 2024-06-12T05:29:04Z | - |
dc.date.issued | 2023-10-23 | - |
dc.identifier.uri | http://pucir.inflibnet.ac.in:8080/jspui/handle/123456789/564 | - |
dc.description.abstract | The 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.iso | en_US | en_US |
dc.subject | carbohydrates; bifunctional thiourea; organocatalyst; enantioselective; Michael addition; aldol reaction | en_US |
dc.title | Synthesis of D-Fructose-Based Bifunctional Primary Amine-Thiourea Organocatalysts and Their Applications in Asymmetric Reactions | en_US |
dc.type | Other | en_US |
Appears in Collections: | Article |
Files in This Item:
File | Description | Size | Format | |
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chemistry-05-00156-v2.pdf | 2.12 MB | Adobe PDF | View/Open |
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