Show simple item record

Files in this item

Thumbnail
Name:
1860_5397_3_18.pdf
Size:
223.8Kb
Format:
PDF
View/Open

A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides

Item metadata

dc.contributor.authorClarke, Matthew L.
dc.contributor.authorFrance, Marcia B.
dc.contributor.authorFuentes, José A.
dc.contributor.authorMilton, Edward J.
dc.contributor.authorRoff, Geoffrey J.
dc.date.accessioned2013-12-05T11:31:03Z
dc.date.available2013-12-05T11:31:03Z
dc.date.issued2007-05-30
dc.identifier651195
dc.identifier9dbb2a1f-6baa-4ad7-8da4-69f22de5991d
dc.identifier000247459500001
dc.identifier34347340382
dc.identifier.citationClarke , M L , France , M B , Fuentes , J A , Milton , E J & Roff , G J 2007 , ' A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides ' , Beilstein Journal of Organic Chemistry , vol. 3 , 18 . https://doi.org/10.1186/1860-5397-3-18en
dc.identifier.otherORCID: /0000-0002-2444-1244/work/59464628
dc.identifier.urihttps://hdl.handle.net/10023/4268
dc.descriptionArticle number 18en
dc.description.abstractA convenient microwave accelerated cross-coupling procedure between aryl chlorides with a range of boronic acids has been developed. An explanation for the low reactivity of highly fluorinated boronic acids in Suzuki coupling is provided.
dc.format.extent4
dc.format.extent229210
dc.language.isoeng
dc.relation.ispartofBeilstein Journal of Organic Chemistryen
dc.subjectII RECEPTOR ANTAGONISTen
dc.subjectFREE HIYAMA REACTIONen
dc.subjectEFFICIENT SYNTHESISen
dc.subjectARYLBORONIC ACIDSen
dc.subjectORGANIC-SYNTHESISen
dc.subjectROOM-TEMPERATUREen
dc.subjectSODIUM-HYDROXIDEen
dc.subjectSTILLE REACTIONen
dc.subjectQD Chemistryen
dc.subject.lccQDen
dc.titleA convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chloridesen
dc.typeJournal articleen
dc.contributor.sponsorEPSRCen
dc.contributor.institutionUniversity of St Andrews. School of Chemistryen
dc.contributor.institutionUniversity of St Andrews. EaSTCHEMen
dc.identifier.doihttps://doi.org/10.1186/1860-5397-3-18
dc.description.statusPeer revieweden
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=34347340382&partnerID=8YFLogxKen
dc.identifier.grantnumberEP/C014545/1en


This item appears in the following Collection(s)

Show simple item record

Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.