Rapid two-step synthesis of drug-like polycyclic substances by sequential multi-catalysis cascade reactions

dc.contributor.author Ramachary, Dhevalapally B.
dc.contributor.author Mondal, Rumpa
dc.contributor.author Venkaiah, Chintalapudi
dc.date.accessioned 2022-03-27T09:40:58Z
dc.date.available 2022-03-27T09:40:58Z
dc.date.issued 2010-01-04
dc.description.abstract An efficient amino acid-/self-/base-/ruthenium-/thermal-catalyzed two-step process for the synthesis of functionalized drug-like carbocycles was achieved through combinations of cascade TCRA/C-allylation/enyne-RCM/Diels-Alder reactions as key steps starting from simple acyclic substrates. In this communication, we report the two-step synthesis of drug-like carbocycles through a combination of organocatalysis with ruthenium-catalysis. © 2010 The Royal Society of Chemistry.
dc.identifier.citation Organic and Biomolecular Chemistry. v.8(2)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/b920152a
dc.identifier.uri http://xlink.rsc.org/?DOI=B920152A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13192
dc.title Rapid two-step synthesis of drug-like polycyclic substances by sequential multi-catalysis cascade reactions
dc.type Journal. Article
dspace.entity.type
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