Evaluation of Baylis–Hillman Routes to 3- (Aminomethyl)coumarin Derivatives

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dc.contributor.authorOlasupo, I
dc.contributor.authorRose, N.R.
dc.contributor.authorKlein, R.
dc.contributor.authorAdams, L.A.
dc.contributor.authorFamiloni, O.B.
dc.contributor.authorKaye, P. T.
dc.date.accessioned2019-08-22T14:24:43Z
dc.date.available2019-08-22T14:24:43Z
dc.date.issued2014
dc.description.abstractThe relative merits of two different Baylis–Hillman approaches toward the preparation of coumarin derivatives, containing peptide-like side chains, have been explored. In one approach, use of methyl acrylate as the activated alkene requires a protecting group strategy, an approach that is not necessary when using tert-butyl acrylate.en_US
dc.description.sponsorshipNational Research Foundation (NRF Grant No. 62273), the Medical Research Council of South Africa (MRC), and Rhodes Universityen_US
dc.identifier.citationDOI: 10.1080/00397911.2013.803575en_US
dc.identifier.issn0039-7911 print=1532-2432 online
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/4618
dc.language.isoenen_US
dc.publisherTaylor & Francis Group, LLCen_US
dc.relation.ispartofseries;44:2
dc.subject3-(Aminomethyl)coumarins; aza-Michael; Baylis–Hillmanen_US
dc.titleEvaluation of Baylis–Hillman Routes to 3- (Aminomethyl)coumarin Derivativesen_US
dc.typeArticleen_US
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