1,6-Conjugate addition of zinc alkyls to para-quinone methides in a continuous-flow microreactor†

dc.contributor.authorJadhav, A.S.
dc.contributor.authorAnand, R.V.
dc.date.accessioned2020-12-04T06:38:15Z
dc.date.available2020-12-04T06:38:15Z
dc.date.issued2017
dc.description.abstractAn efficient method for the synthesis of alkyl diarylmethanes through the 1,6-conjugate addition of dialkylzinc reagents to para-quinone methides (p-QMs) has been developed under continuous flow conditions using a microreactor. This protocol allows to access unsymmetrical alkyl diarylmethanes in moderate to excellent yields using a wide range of p-QMs and dialkylzinc reagents. Interestingly, this transformation worked well without the requirement of a catalyst.en_US
dc.identifier.citationOrganic and Biomolecular Chemistry, 15(1), pp. 56-60.en_US
dc.identifier.otherhttps://doi.org/10.1039/C6OB02277D
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2017/ob/c6ob02277d#!divAbstract
dc.identifier.urihttp://hdl.handle.net/123456789/2663
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectDialkylzincen_US
dc.subjectEfficienten_US
dc.subjectSynthesisen_US
dc.title1,6-Conjugate addition of zinc alkyls to para-quinone methides in a continuous-flow microreactor†en_US
dc.typeArticleen_US

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