Please use this identifier to cite or link to this item: http://hdl.handle.net/10311/1151
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMasesane, I.B.-
dc.contributor.authorDesta, Z.Y.-
dc.date.accessioned2013-08-07T09:34:04Z-
dc.date.available2013-08-07T09:34:04Z-
dc.date.issued2012-
dc.identifier.citationMasesane, I.B. & Desta, Z.Y. (2012) Reactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivatives, Beilstein Journal of Organic Chemistry, Vol. 8, pp. 2166–2175.en_US
dc.identifier.urihttp://hdl.handle.net/10311/1151-
dc.description.abstractThe reported methodologies for the synthesis of chromane derivatives through the reaction of salicylaldehyde and enolates are discussed. The enolates and their equivalents involved in the reactions discussed in this article were derived from ketones, nitroalkanes, malononitrile and α,β-unsaturated compounds.en_US
dc.language.isoenen_US
dc.publisherBeilstein-Institut, https://www.beilstein-journals.org/bjoc/home/home.htmen_US
dc.subjectAcetophenoneen_US
dc.subjectChromaneen_US
dc.subjectEnolatesen_US
dc.subjectMalononitrileen_US
dc.subjectMichael additionen_US
dc.subjectSalicylaldehydeen_US
dc.titleReactions of salicylaldehyde and enolates or their equivalents: versatile synthetic routes to chromane derivativesen_US
dc.typePublished Articleen_US
dc.linkhttps://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-8-244.pdfen_US
Appears in Collections:Research articles (Dept of Chemistry)

Files in This Item:
File Description SizeFormat 
Masesane_BJOC_2012.pdf501.72 kBAdobe PDFThumbnail
View/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.