Di- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols†

dc.contributor.authorDhiman, Seema
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-12-07T06:18:26Z
dc.date.available2020-12-07T06:18:26Z
dc.date.issued2013
dc.description.abstractAn efficient synthetic approach to diheteroarylmethanes and 1,3-diheteroarylpropenes has been developed via Yb(III)-catalyzed sequential self-condensation of 2-furfuryl (or 2-thienyl or 3-indolyl) alcohols followed by intramolecular Friedel–Crafts type reaction and elimination of an aldehyde. This method offers a powerful entry and a potential alternative to the traditional synthesis of diheteroarylalkanes, which are precursors to the synthesis of several intriguing heteroaryls and more significantly, to the synthesis of biofuels.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry,11(46),pp.8030-8035.en_US
dc.identifier.otherhttps://doi.org/10.1039/C3OB41945B
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2013/ob/c3ob41945b#!divAbstract
dc.identifier.urihttp://hdl.handle.net/123456789/2722
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectEfficienten_US
dc.subjectSynthetic approachen_US
dc.subjectAlcoholsen_US
dc.titleDi- and triheteroarylalkanes via self-condensation and intramolecular Friedel–Crafts type reaction of heteroaryl alcohols†en_US
dc.typeArticleen_US

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