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dc.contributor.authorBhattacharyya, Pravat
dc.contributor.authorWoollins, John Derek
dc.date.accessioned2011-04-04T09:34:44Z
dc.date.available2011-04-04T09:34:44Z
dc.date.issued2001-08-20
dc.identifier.citationBhattacharyya , P & Woollins , J D 2001 , ' Selenocarbonyl synthesis using Woollins Reagent ' Tetrahedron Letters , vol. 42 , no. 34 , pp. 5949-5951 . https://doi.org/10.1016/S0040-4039(01)01113-3en
dc.identifier.issn0040-4039
dc.identifier.otherPURE: 5673224
dc.identifier.otherPURE UUID: 0518146b-5258-4296-9084-c9f134644e3c
dc.identifier.otherWOS: 000170376800040
dc.identifier.otherScopus: 0035920859
dc.identifier.otherORCID: /0000-0002-1498-9652/work/31779295
dc.identifier.urihttp://hdl.handle.net/10023/1776
dc.descriptionThis work was funded by EPSRCen
dc.description.abstract[PhP(Se)(mu -Se)](2) selenates secondary and tertiary amides to the corresponding selenoamides in 30-70% yields at 130 degreesC in toluene and indolizine-3-aldehydes to selenoaldehydes in 40-59% yield at 25 degreesC. (C) 2001 Elsevier Science Ltd. All rights reserved.
dc.language.isoeng
dc.relation.ispartofTetrahedron Lettersen
dc.rightsThis is the author's version of an article published in Tetrahedron Letters, available from http://www.sciencedirect.comen
dc.subjectSelenoamideen
dc.subjectSelenoaldehydeen
dc.subjectSelenationen
dc.subjectWoollins reagenten
dc.subjectTelluroamidesen
dc.subjectSelenoamidesen
dc.subjectSelenideen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleSelenocarbonyl synthesis using Woollins Reagenten
dc.typeJournal articleen
dc.description.versionPostprinten
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1016/S0040-4039(01)01113-3
dc.description.statusPeer revieweden


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