Rawal's catalyst as an effective stimulant for the highly asymmetric Michael addition of β-keto esters to functionally rich nitro-olefins

dc.contributor.author Suresh Kumar, A.
dc.contributor.author Prabhakar Reddy, T.
dc.contributor.author Madhavachary, R.
dc.contributor.author Ramachary, Dhevalapally B.
dc.date.accessioned 2022-03-27T09:39:02Z
dc.date.available 2022-03-27T09:39:02Z
dc.date.issued 2016-01-01
dc.description.abstract A general approach to asymmetric synthesis of highly substituted dihydroquinolines was achieved through neighboring ortho-amino group engaged sequential Michael/amination/dehydration reactions on (E)-2-(2-nitrovinyl)anilines with cyclic and acyclic β-keto esters in the presence of a catalytic amount of Rawal's quinidine-NH-benzyl squaramide followed by TFA.
dc.identifier.citation Organic and Biomolecular Chemistry. v.14(24)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c5ob02178b
dc.identifier.uri http://xlink.rsc.org/?DOI=C5OB02178B
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13156
dc.title Rawal's catalyst as an effective stimulant for the highly asymmetric Michael addition of β-keto esters to functionally rich nitro-olefins
dc.type Journal. Article
dspace.entity.type
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