| dc.contributor.author | Kostenko, Nataliya | |
| dc.contributor.author | Eriksson, Anna Cecilia | |
| dc.contributor.author | Engqvist, Stig Olov Magnus | |
| dc.contributor.author | Villa Gonzalez, Susana | |
| dc.contributor.author | Bayer, Annette | |
| dc.date.accessioned | 2016-09-14T07:15:26Z | |
| dc.date.accessioned | 2016-10-11T11:45:48Z | |
| dc.date.available | 2016-09-14T07:15:26Z | |
| dc.date.available | 2016-10-11T11:45:48Z | |
| dc.date.issued | 2013 | |
| dc.identifier.citation | European Journal of Organic Chemistry 2013, 2013(22):4756-4759 | nb_NO |
| dc.identifier.issn | 1099-0690 | |
| dc.identifier.uri | http://hdl.handle.net/11250/2414230 | |
| dc.description.abstract | A new Negishi-type cross-coupling of 2-bromophosphinine has been developed. The new method expands the scope of palladium-catalyzed couplings to monobromophosphinines, which have been considered as poor substrates so far. Moreover, aryl-, alkenyl-, and alkynylzinc bromides were found to be effective coupling partners. | nb_NO |
| dc.language.iso | eng | nb_NO |
| dc.publisher | ChemPubSoc Europe | nb_NO |
| dc.title | Palladium(0)-Catalyzed Cross-Couplings of 2-Bromophosphinine | nb_NO |
| dc.type | Journal article | nb_NO |
| dc.type | Peer reviewed | nb_NO |
| dc.date.updated | 2016-09-14T07:15:26Z | |
| dc.source.journal | European Journal of Organic Chemistry | nb_NO |
| dc.identifier.doi | 10.1002/ejoc.201300710 | |
| dc.identifier.cristin | 1038747 | |
| dc.description.localcode | © 2013 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the authors' accepted and refereed manuscript to the article. | nb_NO |
