Copper-catalyzed hydroarylation of alkynes for the synthesis of fascaplysin, rutacarpine and granulatimide analogues

dc.contributor.author Ramesh, Subburethinam
dc.contributor.author Nagarajan, Rajagopal
dc.date.accessioned 2022-03-27T08:39:58Z
dc.date.available 2022-03-27T08:39:58Z
dc.date.issued 2015-11-17
dc.description.abstract An efficient copper-catalyzed π-activation protocol has been developed for the intramolecular hydroarylation of alkynes. The strategy has been used in atom-economical syntheses of β-carboline analogues. The cycloisomerized products were obtained in moderate to good yields.
dc.identifier.citation Synthesis (Germany). v.47(22)
dc.identifier.issn 00397881
dc.identifier.uri 10.1055/s-0034-1378735
dc.identifier.uri http://www.thieme-connect.de/DOI/DOI?10.1055/s-0034-1378735
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/11422
dc.subject alkynes
dc.subject arylations
dc.subject carbolines
dc.subject cyclizations
dc.title Copper-catalyzed hydroarylation of alkynes for the synthesis of fascaplysin, rutacarpine and granulatimide analogues
dc.type Journal. Article
dspace.entity.type
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