Gold(i) catalysed sequential dehydrative cyclisation/intermolecular [4 + 2] cycloaddition of alkynyldienols onto activated alkynes/alkenes: a facile route to substituted norbornadienes/norbornenes

dc.contributor.author Uruvakili, Anasuyamma
dc.contributor.author Gangadhararao, G.
dc.contributor.author Kumara Swamy, K. C.
dc.date.accessioned 2022-03-27T09:49:15Z
dc.date.available 2022-03-27T09:49:15Z
dc.date.issued 2015-08-21
dc.description.abstract One-pot synthesis of highly substituted norbornadienes/norbornenes via gold-catalysed dehydrative cyclisation of alkynyldienols, followed by intermolecular [4 + 2] cycloaddition of in situ generated cyclopentadiene and activated alkynes/alkenes is described. The precursors, alkynyldienols, are obtained via sequential Sonogashira cross-coupling of 3-bromoenals, alkyne addition and reduction. Yields of the enynals and multisubstituted norbornadienes in all the cases are good to excellent.
dc.identifier.citation Organic and Biomolecular Chemistry. v.13(39)
dc.identifier.issn 14770520
dc.identifier.uri 10.1039/c5ob01458a
dc.identifier.uri http://xlink.rsc.org/?DOI=C5OB01458A
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13339
dc.title Gold(i) catalysed sequential dehydrative cyclisation/intermolecular [4 + 2] cycloaddition of alkynyldienols onto activated alkynes/alkenes: a facile route to substituted norbornadienes/norbornenes
dc.type Journal. Article
dspace.entity.type
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