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