dc.contributor.author | Wang, Chenyang | |
dc.contributor.author | Wang, Xianliang | |
dc.contributor.author | Kong, Deshen | |
dc.contributor.author | Truong, Khai-Nghi | |
dc.contributor.author | Rissanen, Kari | |
dc.contributor.author | Bolm, Carsten | |
dc.date.accessioned | 2022-08-25T11:51:23Z | |
dc.date.available | 2022-08-25T11:51:23Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Wang, 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.other | CONVID_151612636 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/82833 | |
dc.description.abstract | Treatment 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.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Wiley | |
dc.relation.ispartofseries | Chemistry: An Asian Journal | |
dc.rights | CC BY 4.0 | |
dc.subject.other | coupling reaction | |
dc.subject.other | onium salt | |
dc.subject.other | sulfoximine | |
dc.subject.other | sulfoxinium | |
dc.subject.other | triflate | |
dc.title | The Preparation of Diaryl Sulfoxonium Triflates and Their Application in Palladium‐Catalyzed Cross‐Coupling Reactions | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-202208254365 | |
dc.contributor.laitos | Kemian laitos | fi |
dc.contributor.laitos | Department of Chemistry | en |
dc.contributor.oppiaine | Orgaaninen kemia | fi |
dc.contributor.oppiaine | Organic Chemistry | en |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 1861-4728 | |
dc.relation.numberinseries | 19 | |
dc.relation.volume | 17 | |
dc.type.version | acceptedVersion | |
dc.rights.copyright | f 4) © 2022 The Authors. Chemistry - An Asian Journal published by Wiley-VCH | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | kemia | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p1801 | |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.1002/asia.202200828 | |
jyx.fundinginformation | C. 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.okm | A1 | |