Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2577
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dc.contributor.authorShirke, R.P.-
dc.contributor.authorReddy, V.-
dc.contributor.authorAnand, R.V.-
dc.contributor.authorRamasastry, S.S.V.-
dc.date.accessioned2020-12-03T09:07:48Z-
dc.date.available2020-12-03T09:07:48Z-
dc.date.issued2016-
dc.identifier.citationSynthesis (Germany), 48(12), pp.1865-1871.en_US
dc.identifier.other10.1055/s-0035-1560432 special topic-
dc.identifier.urihttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0035-1560432-
dc.identifier.urihttp://hdl.handle.net/123456789/2577-
dc.description.abstractThe first synthesis of dihydrobenzofuranones and benzofurans based on an intramolecular cross-benzoin reaction has been reported. Commercially available 3-furan carboxaldehydes are readily α-alkylated to furnish 3-formyl-2-furylcarbinols, which are further elaborated to the synthesis of benzofurans in good yields through sequential bismuth(III) chloride catalysed furfurylation and a novel NHC-promoted intramolecular cross-benzoin condensation reaction.en_US
dc.language.isoenen_US
dc.publisherThiemeen_US
dc.subjectN-heterocyclic carbenesen_US
dc.subjectOrganocatalysisen_US
dc.subjectAnnulationen_US
dc.subjectBenzoin condensationen_US
dc.titleFurans to Benzofurans: Intramolecular Cross-Benzoin Reactions Catalysed by N-Heterocyclic Carbenesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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