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Halide exchanged Hoveyda-type complexes in olefin metathesis
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dc.contributor.author | Wappel, Julia | |
dc.contributor.author | Urbina-Blanco, Cesar A. | |
dc.contributor.author | Abbas, Mudassar | |
dc.contributor.author | Albering, Joerg H. | |
dc.contributor.author | Saf, Robert | |
dc.contributor.author | Nolan, Steven P. | |
dc.contributor.author | Slugovc, Christian | |
dc.date.accessioned | 2013-12-04T15:31:01Z | |
dc.date.available | 2013-12-04T15:31:01Z | |
dc.date.issued | 2010-11 | |
dc.identifier | 5496037 | |
dc.identifier | 5be10a20-512c-46f5-a63f-d34df8bb974d | |
dc.identifier | 000284527400002 | |
dc.identifier | 78751487069 | |
dc.identifier.citation | Wappel , J , Urbina-Blanco , C A , Abbas , M , Albering , J H , Saf , R , Nolan , S P & Slugovc , C 2010 , ' Halide exchanged Hoveyda-type complexes in olefin metathesis ' , Beilstein Journal of Organic Chemistry , vol. 6 , pp. 1091-1098 . https://doi.org/10.3762/bjoc.6.125 | en |
dc.identifier.uri | https://hdl.handle.net/10023/4261 | |
dc.description.abstract | The aims of this contribution are to present a straightforward synthesis of 2(nd) generation Hoveyda-type olefin metathesis catalysts bearing bromo and iodo ligands, and to disclose the subtle influence of the different anionic co-ligands on the catalytic performance of the complexes in ring opening metathesis polymerisation, ring closing metathesis, enyne cycloisomerisation and cross metathesis reactions. | |
dc.format.extent | 8 | |
dc.format.extent | 1442529 | |
dc.language.iso | eng | |
dc.relation.ispartof | Beilstein Journal of Organic Chemistry | en |
dc.subject | Cross metathesis | en |
dc.subject | Olefin metathesis | en |
dc.subject | RCM | en |
dc.subject | ROMP | en |
dc.subject | Ruthenium | en |
dc.subject | QD Chemistry | en |
dc.subject.lcc | QD | en |
dc.title | Halide exchanged Hoveyda-type complexes in olefin metathesis | en |
dc.type | Journal article | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.contributor.institution | University of St Andrews. EaSTCHEM | en |
dc.identifier.doi | https://doi.org/10.3762/bjoc.6.125 | |
dc.description.status | Peer reviewed | en |
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