Towards organo-click reactions: development of pharmaceutical ingredients by using direct organocatalytic bio-mimetic reductions

Ramachary, Dhevalapally B. ; Reddy, G. Babul (2006) Towards organo-click reactions: development of pharmaceutical ingredients by using direct organocatalytic bio-mimetic reductions Organic and Biomolecular Chemistry, 4 (24). p. 4463. ISSN 1477-0520

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Official URL: http://doi.org/10.1039/B612611A

Related URL: http://dx.doi.org/10.1039/B612611A

Abstract

Economic and environmentally friendly bio-mimetic one-pot three and four-component Knoevenagel–hydrogenation (K–H), five-component Knoevenagel–hydrogenation–alkylation (K–H–A) and six-component Knoevenagel–hydrogenation–alkylation–Huisgen cycloaddition (K–H–A–HC) reactions of aldehydes, CH-acids, o-phenylenediamine, alkyl halides and azides using proline, proline–metal carbonate and proline–metal carbonate–CuI-catalysis, respectively have been developed. Many of K–H and K–H–A compounds have direct application in pharmaceutical chemistry.

Item Type:Article
Source:Copyright of this article belongs to The Royal Society of Chemistry.
ID Code:120790
Deposited On:05 Jul 2021 08:07
Last Modified:05 Jul 2021 08:07

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