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Synthesis and selenation of tandem multicomponent condensation adducts

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dc.contributor.authorHua, Guoxiong
dc.contributor.authorDu, Junyi
dc.contributor.authorFuller, Amy
dc.contributor.authorAthukorala Arachchige, Kasun Sankalpa
dc.contributor.authorCordes, David Bradford
dc.contributor.authorSlawin, Alexandra Martha Zoya
dc.contributor.authorWoollins, J Derek
dc.date.accessioned2016-02-03T00:11:51Z
dc.date.available2016-02-03T00:11:51Z
dc.date.issued2015
dc.identifier166277084
dc.identifier01e571be-36d9-4378-a7c1-2e42ca344034
dc.identifier84925517869
dc.identifier000351583700023
dc.identifier.citationHua , G , Du , J , Fuller , A , Athukorala Arachchige , K S , Cordes , D B , Slawin , A M Z & Woollins , J D 2015 , ' Synthesis and selenation of tandem multicomponent condensation adducts ' , Synlett , vol. In press . https://doi.org/10.1055/s-0034-1380124en
dc.identifier.issn0936-5214
dc.identifier.otherORCID: /0000-0002-5366-9168/work/28024012
dc.identifier.otherORCID: /0000-0002-9527-6418/work/56861783
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779185
dc.identifier.urihttps://hdl.handle.net/10023/8119
dc.description.abstractA number of four-component condensation adducts, which were readily obtained from one-pot reaction of aryl carboxylic acids, arylaldehydes, arylamines and c-hexylisocyanide, were treated with two equivalents of Woollins’ reagent leading to the formation of a series of novel selenoamides with one or two C=Se groups, or heterocyclic compounds such as 1,3-selenazole and 1,3-selenazolidin-5-one
dc.format.extent703788
dc.language.isoeng
dc.relation.ispartofSynletten
dc.subjectOne-pot reactionen
dc.subjectMulticomponent condensation adductsen
dc.subjectWoollins’ reagenten
dc.subjectSelenoamidesen
dc.subjectSelenium-nitrogen heterocyclesen
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleSynthesis and selenation of tandem multicomponent condensation adductsen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.contributor.institutionUniversity of St Andrews. Office of the Principalen
dc.identifier.doi10.1055/s-0034-1380124
dc.description.statusPeer revieweden
dc.date.embargoedUntil2016-02-03
dc.identifier.urlhttps://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0034-1380124#supmaten
dc.identifier.grantnumberEP/K503940/1en
dc.identifier.grantnumberEP/K031252/1en
dc.identifier.grantnumberEP/K039210/1en


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