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dc.contributor.authorMazimba, O.
dc.contributor.authorMasesane, I.B.
dc.contributor.authorMajinda, R.R.
dc.date.accessioned2012-08-08T07:51:35Z
dc.date.available2012-08-08T07:51:35Z
dc.date.issued2011
dc.identifier.citationMazimba, O. et al (2011) An efficient synthesis of flavans from salicylaldehyde and acetophenone derivatives, Tetrahedron Letters, Vol. 52, No. 50, pp. 6716–6718en_US
dc.identifier.issn0040-4039
dc.identifier.urihttp://hdl.handle.net/10311/1027
dc.description.abstractAn efficient total synthesis of flavans from the reactions of salicylaldehyde and acetophenone derivatives is reported. The synthesis involves preparation of chalcones through an aldol reaction followed by reduction of both the double bond and the ketone using NaBH4 and an acetic acid mediated cyclization. Methoxy groups on the aromatic rings did not affect significantly the yields of the procedure.en_US
dc.language.isoenen_US
dc.publisherElsevier Science Ltd, http://www.elsevier.com/locate/tetleten_US
dc.subjectFlavanen_US
dc.subjectAcetophenoneen_US
dc.subjectSalicylaldehydeen_US
dc.subjectAldol condensationen_US
dc.subjectReductionen_US
dc.titleAn efficient synthesis of flavans from salicylaldehyde and acetophenone derivativesen_US
dc.typePublished Articleen_US
dc.linkhttp://ac.els-cdn.com/S0040403911017023/1-s2.0-S0040403911017023-main.pdf?_tid=96c1b321c39be9004114565db90e546b&acdnat=1343895392_4106dd1da3300866fe3722c70fad6992en_US


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