Resorcinarene-Functionalised Imidazolium Salts as Ligand Precursors for Palladium-Catalysed SuzukiMiyaura Cross-Couplings
dc.authorid | Özdemir, İsmail/0000-0001-6325-0216 | |
dc.authorwosid | TOUPET, Loic/N-7043-2014 | |
dc.authorwosid | ŞAHİN, Neslihan/F-6402-2019 | |
dc.authorwosid | Özdemir, İsmail/ABI-5192-2020 | |
dc.contributor.author | Sahin, Neslihan | |
dc.contributor.author | Semeril, David | |
dc.contributor.author | Brenner, Eric | |
dc.contributor.author | Matt, Dominique | |
dc.contributor.author | Ozdemir, Ismail | |
dc.contributor.author | Kaya, Cemal | |
dc.contributor.author | Toupet, Loic | |
dc.date.accessioned | 2024-08-04T20:37:34Z | |
dc.date.available | 2024-08-04T20:37:34Z | |
dc.date.issued | 2013 | |
dc.department | İnönü Üniversitesi | en_US |
dc.description.abstract | Three imidazolium salts based on a rigid resorcinarene platform (13) were synthesised and used as catalyst precursors in the SuzukiMiyaura cross-coupling of aryl halides with phenylboronic acid. In these pro-carbene ligands, the heterocyclic moiety has one N atom connected to a C2 atom of a resorcinolic ring, and the other is substituted by an alkyl group (R=n-propyl, iso-propyl, benzyl). The methinic C atoms of the macrocyclic core are all substituted by a pentyl group. The best catalytic performances were obtained by using an imidazolium/Pd ratio of 1:1. The catalytic systems displayed high activities, which increased in the order R=n-propyl(1) | en_US |
dc.description.sponsorship | scientific and technological research of Turkey (TUBITAK-BIDEB); International Research Fellowship Programme | en_US |
dc.description.sponsorship | The authors thank the scientific and technological research of Turkey (TUBITAK-BIDEB) and the International Research Fellowship Programme for the grant to N.S. Grateful acknowledgement is due to Johnson Matthey for a loan of palladium. | en_US |
dc.identifier.doi | 10.1002/cctc.201200716 | |
dc.identifier.endpage | 1125 | en_US |
dc.identifier.issn | 1867-3880 | |
dc.identifier.issn | 1867-3899 | |
dc.identifier.issue | 5 | en_US |
dc.identifier.scopus | 2-s2.0-84877057982 | en_US |
dc.identifier.scopusquality | Q1 | en_US |
dc.identifier.startpage | 1116 | en_US |
dc.identifier.uri | https://doi.org/10.1002/cctc.201200716 | |
dc.identifier.uri | https://hdl.handle.net/11616/96044 | |
dc.identifier.volume | 5 | en_US |
dc.identifier.wos | WOS:000318240600013 | en_US |
dc.identifier.wosquality | Q1 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Wiley-V C H Verlag Gmbh | en_US |
dc.relation.ispartof | Chemcatchem | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | cavitands | en_US |
dc.subject | carbenes | en_US |
dc.subject | palladium | en_US |
dc.subject | nitrogen heterocycles | en_US |
dc.subject | cross-coupling | en_US |
dc.title | Resorcinarene-Functionalised Imidazolium Salts as Ligand Precursors for Palladium-Catalysed SuzukiMiyaura Cross-Couplings | en_US |
dc.type | Article | en_US |