Gold(I)-catalyzed 6-endo-dig hydrative cyclization of an alkyne-tethered ynamide: Access to 1,6-dihydropyridin-2(3H)ones

dc.contributor.author Ghosh, Nayan
dc.contributor.author Nayak, Sanatan
dc.contributor.author Sahoo, Akhila K.
dc.date.accessioned 2022-03-27T08:34:19Z
dc.date.available 2022-03-27T08:34:19Z
dc.date.issued 2013-07-15
dc.description.abstract Hydrate your chemistry! Hydrative cyclization of 5-yne-ynamides in the presence of Echavarren's catalyst and p-toluenesulphonic acid (PTSA)×H2O at room temperature affords an array of 1,6-dihydropyridin-2(3H)one derivatives. Isomerization, epoxidation, and hydrogenation of the double bond and insertion of an extended π-conjugate system into the pyridinone skeleton have been successfully accomplished (see scheme; Ts=tosyl). Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.identifier.citation Chemistry - A European Journal. v.19(29)
dc.identifier.issn 09476539
dc.identifier.uri 10.1002/chem.201301599
dc.identifier.uri https://onlinelibrary.wiley.com/doi/10.1002/chem.201301599
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/10915
dc.subject gold catalysis
dc.subject heterocycles
dc.subject hydrative cyclization
dc.subject pyridinones
dc.subject yne-ynamides
dc.title Gold(I)-catalyzed 6-endo-dig hydrative cyclization of an alkyne-tethered ynamide: Access to 1,6-dihydropyridin-2(3H)ones
dc.type Journal. Article
dspace.entity.type
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