Facile Access to Cyclopentadienes via Catalytic Intramolecular Palladium-Ene Reaction of 2,4-Pentadienyl Acetates

dc.contributor.authorBharadwaj, S.K.
dc.contributor.authorBankar, S.K.
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-11-26T06:40:48Z
dc.date.available2020-11-26T06:40:48Z
dc.date.issued2018
dc.description.abstractWe have recently disclosed a palladium-catalyzed Trost–­Oppolzer type Alder-ene reaction of 2,4-pentadienyl acetates for the synthesis of highly substituted cyclopentadienes and cyclopentene-fused aromatics. The overall transformation also represents an acid-free iso-Nazarov type cyclization. Herein, we provide the hypothesis and ­rationale behind this work, while highlighting the seminal contributions of Trost, Oppolzer and others towards the development of the palladium-ene reaction.en_US
dc.identifier.citationSynlett, 29(19), pp. 2456-2460en_US
dc.identifier.otherDOI: 10.1055/s-0037-1610552
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0037-1610552
dc.identifier.urihttp://hdl.handle.net/123456789/2260
dc.language.isoenen_US
dc.publisherGeorg Thieme Verlagen_US
dc.subjectTsuji–Trost reactionen_US
dc.subjectMetallo-ene reactionen_US
dc.subjectCyclopentanesen_US
dc.subjectIso-Nazarov ­reactionen_US
dc.subjectAnnulationen_US
dc.titleFacile Access to Cyclopentadienes via Catalytic Intramolecular Palladium-Ene Reaction of 2,4-Pentadienyl Acetatesen_US
dc.typeArticleen_US

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