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dc.contributor.authorNIKOLAIENKO, Pavlo
dc.contributor.authorRUEPING, Magnus
dc.contributor.authorYildiz, Tülay
dc.date.accessioned2021-03-05T18:32:58Z
dc.date.available2021-03-05T18:32:58Z
dc.date.issued2016
dc.identifier.citationNIKOLAIENKO 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.issn1434-193X
dc.identifier.otherav_cadd5ff8-269b-4e5f-9ca0-8277f3affb6a
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/134400
dc.identifier.urihttps://doi.org/10.1002/ejoc.201501623
dc.description.abstractThe 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.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.subjectBiyoinorganik Kimya
dc.subjectKimya
dc.subjectKİMYA, ORGANİK
dc.titleTrifluoromethylthiolation of Unsymmetrical lambda(3)-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRY
dc.contributor.departmentRWTH Aachen University , ,
dc.identifier.volume2016
dc.identifier.issue6
dc.identifier.startpage1091
dc.identifier.endpage1094
dc.contributor.firstauthorID77333


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