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

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Reddy, G. Babul
dc.date.accessioned 2022-03-27T09:42:04Z
dc.date.available 2022-03-27T09:42:04Z
dc.date.issued 2006-12-07
dc.description.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-Cu I-catalysis, respectively have been developed. Many of K-H and K-H-A compounds have direct application in pharmaceutical chemistry. © The Royal Society of Chemistry.
dc.identifier.citation Organic and Biomolecular Chemistry. v.4(24)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/b612611a
dc.identifier.uri http://xlink.rsc.org/?DOI=b612611a
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13212
dc.title Towards organo-click reactions: Development of pharmaceutical ingredients by using direct organocatalytic bio-mimetic reductions
dc.type Journal. Article
dspace.entity.type
Files
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Plain Text
Description: