dc.contributor.author | NIKOLAIENKO, Pavlo | |
dc.contributor.author | RUEPING, Magnus | |
dc.contributor.author | Yildiz, Tülay | |
dc.date.accessioned | 2021-03-05T18:32:58Z | |
dc.date.available | 2021-03-05T18:32:58Z | |
dc.date.issued | 2016 | |
dc.identifier.citation | NIKOLAIENKO P., Yildiz T., RUEPING M., "Trifluoromethylthiolation of Unsymmetrical lambda(3)-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group", EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, cilt.2016, ss.1091-1094, 2016 | |
dc.identifier.issn | 1434-193X | |
dc.identifier.other | av_cadd5ff8-269b-4e5f-9ca0-8277f3affb6a | |
dc.identifier.other | vv_1032021 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/134400 | |
dc.identifier.uri | https://doi.org/10.1002/ejoc.201501623 | |
dc.description.abstract | The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward pathway for the synthesis of aryl trifluoromethyl thioethers under mild reaction conditions and within short reaction times. High chemoselectivity was achieved by using mesityl as a leaving group. A large range of novel [(het)aryl](mesityl)iodonium salts underwent this reaction under the optimized conditions to give the desired products in moderate to good yields. | |
dc.language.iso | eng | |
dc.subject | Temel Bilimler (SCI) | |
dc.subject | Biyokimya | |
dc.subject | Temel Bilimler | |
dc.subject | Biyoinorganik Kimya | |
dc.subject | Kimya | |
dc.subject | KİMYA, ORGANİK | |
dc.title | Trifluoromethylthiolation of Unsymmetrical lambda(3)-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group | |
dc.type | Makale | |
dc.relation.journal | EUROPEAN JOURNAL OF ORGANIC CHEMISTRY | |
dc.contributor.department | RWTH Aachen University , , | |
dc.identifier.volume | 2016 | |
dc.identifier.issue | 6 | |
dc.identifier.startpage | 1091 | |
dc.identifier.endpage | 1094 | |
dc.contributor.firstauthorID | 77333 | |