Gold-catalyzed intermolecular hydrophenoxylation of unactivated Internal alkynes

dc.contributor.author Kuram, Malleswara Rao
dc.contributor.author Bhanuchandra, M.
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T08:35:04Z
dc.date.available 2022-03-27T08:35:04Z
dc.date.issued 2010-04-02
dc.description.abstract Chemical Reaction Reprentation A general and simple strategy for the synthesis of functionally diverse arylvinyl ethers is reported through gold-catalyzed intermolecular addition of electronically and sterically substituted phenols with unactivated alkynes. Addition of phenols to unsymmetrical alkynes provides the corresponding mixture of regioisomers with appreciable selectivity. Multiple hydrophenoxylations of polyphenols with diphenylacetylene are demonstrated successfully. © 2010 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.75(7)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo1000143
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo1000143
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11026
dc.title Gold-catalyzed intermolecular hydrophenoxylation of unactivated Internal alkynes
dc.type Journal. Article
dspace.entity.type
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