Show simple item record

Files in this item


Item metadata

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.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 .
dc.identifier.otherPURE: 166277084
dc.identifier.otherPURE UUID: 01e571be-36d9-4378-a7c1-2e42ca344034
dc.identifier.otherScopus: 84925517869
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.otherWOS: 000351583700023
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.rights© Georg Thieme Verlag Stuttgart · New York. This work is made available online in accordance with the publisher’s policies. This is the author created, accepted version manuscript following peer review and may differ slightly from the final published version. The final published version of this work is available at
dc.subjectOne-pot reactionen
dc.subjectMulticomponent condensation adductsen
dc.subjectWoollins’ reagenten
dc.subjectSelenium-nitrogen heterocyclesen
dc.subjectQD Chemistryen
dc.titleSynthesis and selenation of tandem multicomponent condensation adductsen
dc.typeJournal articleen
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.description.statusPeer revieweden

This item appears in the following Collection(s)

Show simple item record