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A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides
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dc.contributor.author | Clarke, Matthew L. | |
dc.contributor.author | France, Marcia B. | |
dc.contributor.author | Fuentes, José A. | |
dc.contributor.author | Milton, Edward J. | |
dc.contributor.author | Roff, Geoffrey J. | |
dc.date.accessioned | 2013-12-05T11:31:03Z | |
dc.date.available | 2013-12-05T11:31:03Z | |
dc.date.issued | 2007-05-30 | |
dc.identifier | 651195 | |
dc.identifier | 9dbb2a1f-6baa-4ad7-8da4-69f22de5991d | |
dc.identifier | 000247459500001 | |
dc.identifier | 34347340382 | |
dc.identifier.citation | Clarke , 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/10.1186/1860-5397-3-18 | en |
dc.identifier.other | ORCID: /0000-0002-2444-1244/work/59464628 | |
dc.identifier.uri | https://hdl.handle.net/10023/4268 | |
dc.description | Article number 18 | en |
dc.description.abstract | A 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.extent | 4 | |
dc.format.extent | 229210 | |
dc.language.iso | eng | |
dc.relation.ispartof | Beilstein Journal of Organic Chemistry | en |
dc.subject | II RECEPTOR ANTAGONIST | en |
dc.subject | FREE HIYAMA REACTION | en |
dc.subject | EFFICIENT SYNTHESIS | en |
dc.subject | ARYLBORONIC ACIDS | en |
dc.subject | ORGANIC-SYNTHESIS | en |
dc.subject | ROOM-TEMPERATURE | en |
dc.subject | SODIUM-HYDROXIDE | en |
dc.subject | STILLE REACTION | en |
dc.subject | QD Chemistry | en |
dc.subject.lcc | QD | en |
dc.title | A convenient catalyst system for microwave accelerated cross-coupling of a range of aryl boronic acids with aryl chlorides | en |
dc.type | Journal article | en |
dc.contributor.sponsor | EPSRC | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | 10.1186/1860-5397-3-18 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | http://www.scopus.com/inward/record.url?scp=34347340382&partnerID=8YFLogxK | en |
dc.identifier.grantnumber | EP/C014545/1 | en |
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