The Baylis–Hillman approach to quinoline derivatives

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dc.contributor.authorFamiloni, O.B.
dc.contributor.authorKlaas, P.J.
dc.contributor.authorLobb, K.A.
dc.contributor.authorPakade, V.E.
dc.contributor.authorKaye, P.T.
dc.date.accessioned2019-08-29T13:27:17Z
dc.date.available2019-08-29T13:27:17Z
dc.date.issued2006-09-25
dc.descriptionStaff Publicationen_US
dc.description.abstractBaylis–Hillman reactions of 2-nitrobenzaldehydes with various activated alkenes afford adducts that undergo reductive cyclisation to quinoline derivatives. The chemo- and regioselectivity of cyclisation appears to be influenced by the choice of both the substrate and the reagent system, and competing reactions have been observed.en_US
dc.identifier.citationFamiloni, O. B., [Et...al] (2006). The Baylis–Hillman approach to quinoline derivatives. Organic & biomolecular chemistry, Vol.4(21), 3960-3965.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/4880
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.relation.ispartofseriesOrganic & biomolecular chemistry;Vol.4(21)
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesisen_US
dc.subjectchemoselectivityen_US
dc.subjectRegioselectivityen_US
dc.subjectBaylis-Hillman reactionsen_US
dc.titleThe Baylis–Hillman approach to quinoline derivativesen_US
dc.typeArticleen_US
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