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dc.contributor.authorWang, Chenyang
dc.contributor.authorWang, Xianliang
dc.contributor.authorKong, Deshen
dc.contributor.authorTruong, Khai-Nghi
dc.contributor.authorRissanen, Kari
dc.contributor.authorBolm, Carsten
dc.date.accessioned2022-08-25T11:51:23Z
dc.date.available2022-08-25T11:51:23Z
dc.date.issued2022
dc.identifier.citationWang, C., Wang, X., Kong, D., Truong, K.-N., Rissanen, K., & Bolm, C. (2022). The Preparation of Diaryl Sulfoxonium Triflates and Their Application in Palladium‐Catalyzed Cross‐Coupling Reactions. <i>Chemistry: An Asian Journal</i>, <i>17</i>(19), Article e202200828. <a href="https://doi.org/10.1002/asia.202200828" target="_blank">https://doi.org/10.1002/asia.202200828</a>
dc.identifier.otherCONVID_151612636
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/82833
dc.description.abstractTreatment of N-methyl-S,S-diaryl sulfoximines with methyl trifluoromethanesulfonate provides bench-stable sulfoxinium salts in excellent yields. Applying them in Sonogashira-, Heck- and Suzuki-type cross-coupling reactions leads to the corresponding products by sequential C–S bond cleavage and C–C bond formation. Electronic factors induced by substituents on the S-aryl groups govern the coupling efficiency.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesChemistry: An Asian Journal
dc.rightsCC BY 4.0
dc.subject.othercoupling reaction
dc.subject.otheronium salt
dc.subject.othersulfoximine
dc.subject.othersulfoxinium
dc.subject.othertriflate
dc.titleThe Preparation of Diaryl Sulfoxonium Triflates and Their Application in Palladium‐Catalyzed Cross‐Coupling Reactions
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202208254365
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.relation.issn1861-4728
dc.relation.numberinseries19
dc.relation.volume17
dc.type.versionacceptedVersion
dc.rights.copyrightf 4) © 2022 The Authors. Chemistry - An Asian Journal published by Wiley-VCH
dc.rights.accesslevelopenAccessfi
dc.subject.ysokemia
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p1801
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/asia.202200828
jyx.fundinginformationC. W., X. W., and D. K. are grateful to the China Scholarship Council for predoctoral stipends. The Alexander von Humboldt Foundation is acknowledged for the high recognition of K. R. (AvH research award).
dc.type.okmA1


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