N-Heterocyclic carbene catalysed 1,6-hydrophosphonylation of p-quinone methides and fuchsones: an atom economical route to unsymmetrical diaryl- and triarylmethyl phosphonates

dc.contributor.authorArde, Panjab
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-03T09:44:46Z
dc.date.available2020-12-03T09:44:46Z
dc.date.issued2016
dc.description.abstractA convenient organocatalytic approach to access unsymmetrical diaryl- and triarylmethyl phosphonates using NHC as a Brønsted base catalyst is described. This atom-economical protocol enables the installation of phosphonate groups on p-quinone methides and fuchsones through a 1,6-conjugate addition of dialkylphosphites, and the corresponding phosphonates were obtained in excellent yields.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 14(24), pp. 5550-5554en_US
dc.identifier.otherDOI: 10.1039/C6OB00289G
dc.identifier.urihttps://pubs.rsc.org/en/content/articlehtml/2016/ob/c6ob00289g
dc.identifier.urihttp://hdl.handle.net/123456789/2591
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectN-Heterocyclicen_US
dc.subjectHydrophosphonylationen_US
dc.subjectOrganocatalyticen_US
dc.subjectPhosphonatesen_US
dc.titleN-Heterocyclic carbene catalysed 1,6-hydrophosphonylation of p-quinone methides and fuchsones: an atom economical route to unsymmetrical diaryl- and triarylmethyl phosphonatesen_US
dc.typeArticleen_US

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