Unprecedented Stereochemical Reversal from Alkyl to Aryl Substituents in the Johnson-Claisen Rearrangement of Methyl 3-Hydroxy-2-methylenealkanoates

dc.contributor.author Basavaiah, D.
dc.contributor.author Pandiaraju, S.
dc.contributor.author Krishnamacharyulu, M.
dc.date.accessioned 2022-03-27T09:04:12Z
dc.date.available 2022-03-27T09:04:12Z
dc.date.issued 1996-01-01
dc.description.abstract An unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates with triethyl orthoacetate with a plausible mechanism has been described.
dc.identifier.citation Synlett. v.1996(8)
dc.identifier.issn 09365214
dc.identifier.uri 10.1055/s-1996-5524
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-1996-5524
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12364
dc.title Unprecedented Stereochemical Reversal from Alkyl to Aryl Substituents in the Johnson-Claisen Rearrangement of Methyl 3-Hydroxy-2-methylenealkanoates
dc.type Journal. Article
dspace.entity.type
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