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.accessioned2019-09-05T09:26:57Z
dc.date.available2019-09-05T09:26:57Z
dc.date.issued2013-10-29
dc.descriptionStaff publicationsen_US
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.identifier.citationOlasupo, I., [Et...al] (2014). Evaluation of Baylis–Hillman Routes to 3-(Aminomethyl) coumarin Derivatives. Synthetic Communications, Vol.44(2), 251-258pp.en_US
dc.identifier.urihttps://ir.unilag.edu.ng/handle/123456789/5143
dc.language.isoenen_US
dc.publisherTaylor & Francis Onlineen_US
dc.subjectResearch Subject Categories::NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesisen_US
dc.subject3-(Aminomethyl)coumarinsen_US
dc.subjectaza-Michaelen_US
dc.subjectBaylis-Hillmanen_US
dc.titleEvaluation of Baylis–Hillman Routes to 3-(Aminomethyl)coumarin Derivativesen_US
dc.typeArticleen_US
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