Direct amino acid-catalyzed cascade reductive alkylation of arylacetonitriles: High-yielding synthesis of ibuprofen analogs

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Shiva Prasad, M.
dc.date.accessioned 2022-03-27T09:40:49Z
dc.date.available 2022-03-27T09:40:49Z
dc.date.issued 2010-10-06
dc.description.abstract A novel approach for a one-pot, three-component reductive alkylation (TCRA) reaction of arylacetonitriles-containing electron-withdrawing groups with aldehydes/ketones and 1,4-dihydropyridine via iminium-catalysis has been developed. Many TCRA reaction products have direct applications in agricultural and pharmaceutical chemistry. © 2010 Elsevier Ltd. All rights reserved.
dc.identifier.citation Tetrahedron Letters. v.51(40)
dc.identifier.issn 00404039
dc.identifier.uri 10.1016/j.tetlet.2010.07.131
dc.identifier.uri https://www.sciencedirect.com/science/article/abs/pii/S0040403910013377
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13189
dc.subject Amino acids
dc.subject Cascade reactions
dc.subject Ibuprofen analogs
dc.subject Organocatalysis
dc.subject TCRA reactions
dc.title Direct amino acid-catalyzed cascade reductive alkylation of arylacetonitriles: High-yielding synthesis of ibuprofen analogs
dc.type Journal. Article
dspace.entity.type
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