Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4835
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dc.contributor.authorMondal, Atanu-
dc.contributor.authorSatpathi, Bishnupada-
dc.contributor.authorRamasastry, S. S. V.-
dc.date.accessioned2023-08-18T10:54:03Z-
dc.date.available2023-08-18T10:54:03Z-
dc.date.issued2021-
dc.identifier.citationOrganic Letters, 24(1), 256–261.en_US
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acs.orglett.1c03913-
dc.identifier.urihttp://hdl.handle.net/123456789/4835-
dc.descriptionOnly IISER Mohali authors are available in the recorden_US
dc.description.abstractWe demonstrate the first phosphine-catalyzed intramolecular vinylogous aldol reaction (IVAR) of α-substituted enones. This strategy provides access to various pentannulated (hetero)arenes and dibenzocycloheptanones incorporated with two contiguous stereocenters, one of which is an all-carbon quaternary center. The scope of this work is further broadened through elaborations of the IVAR adducts to (i) benzannulated nine-membered carbocyclic systems, (ii) interesting classes of 1,3-dienes, 1,3,5-trienes, and 1-yn-3,5-dienes, and (iii) the analogs of echinolactone D and russujaponol F.en_US
dc.language.isoen_USen_US
dc.publisherACS Publicationsen_US
dc.subjectAdductsen_US
dc.subjectChemical reactionsen_US
dc.titlePhosphine-Catalyzed Intramolecular Vinylogous Aldol Reaction of α-Substituted Enonesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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