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Synthesis of (diarylmethyl)amines using Ni-catalyzed arylation of C(sp3)-H bonds
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dc.contributor.author | Fernandez Salas, Jose Antonio | |
dc.contributor.author | Marelli, Enrico | |
dc.contributor.author | Nolan, Steven Patrick | |
dc.date.accessioned | 2015-07-22T08:40:04Z | |
dc.date.available | 2015-07-22T08:40:04Z | |
dc.date.issued | 2015-08-01 | |
dc.identifier | 204333631 | |
dc.identifier | e5876da8-388b-4336-98b5-3d6f40717de8 | |
dc.identifier | 84937239249 | |
dc.identifier | 000357931700072 | |
dc.identifier.citation | Fernandez Salas , J A , Marelli , E & Nolan , S P 2015 , ' Synthesis of (diarylmethyl)amines using Ni-catalyzed arylation of C(sp 3 )-H bonds ' , Journal of Polymer Science Part A: Polymer Chemistry , vol. 6 , no. 8 , pp. 4973-4977 . https://doi.org/10.1039/C5SC01589H | en |
dc.identifier.issn | 0887-624X | |
dc.identifier.other | Bibtex: urn:3cde3db584f67c593669c88edd6941f3 | |
dc.identifier.uri | https://hdl.handle.net/10023/7008 | |
dc.description | The authors thank the ERC (Advanced Researcher award-FUNCAT), the EPSRC (grant no EP/J011053/1) and King Saud University for funding. SPN is a Royal Society Wolfson Research Merit Award holder. | en |
dc.description.abstract | The first nickel catalyzed deprotonative cross coupling between C(sp3)-H bonds and aryl chlorides is reported, allowing the challenging arylation of benzylimines in the absence of directing group or stoichiometric metal activation. This methodology represents a convenient access to the (diarylmethyl)amine moiety, which is widespread in pharmaceutically relevant compounds. | |
dc.format.extent | 5 | |
dc.format.extent | 504407 | |
dc.language.iso | eng | |
dc.relation.ispartof | Journal of Polymer Science Part A: Polymer Chemistry | en |
dc.subject | QD Chemistry | en |
dc.subject | NDAS | en |
dc.subject.lcc | QD | en |
dc.title | Synthesis of (diarylmethyl)amines using Ni-catalyzed arylation of C(sp3)-H bonds | en |
dc.type | Journal article | en |
dc.contributor.sponsor | European Research Council | 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 | https://doi.org/10.1039/C5SC01589H | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | http://www.rsc.org/suppdata/c5/sc/c5sc01589h/c5sc01589h1.pdf | en |
dc.identifier.grantnumber | FP7-227817 FUNCAT | en |
dc.identifier.grantnumber | EP/J011053/1 | en |
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