dc.contributor.author | Wu, Peng | |
dc.contributor.author | Ward, Jas S. | |
dc.contributor.author | Rissanen, Kari | |
dc.contributor.author | Bolm, Carsten | |
dc.date.accessioned | 2023-02-27T11:02:10Z | |
dc.date.available | 2023-02-27T11:02:10Z | |
dc.date.issued | 2023 | |
dc.identifier.citation | Wu, P., Ward, J. S., Rissanen, K., & Bolm, C. (2023). Cyclic Sulfoximine and Sulfonimidamide Derivatives by Copper‐Catalyzed Cross‐Coupling Reactions with Elemental Sulfur. <i>Advanced Synthesis and Catalysis</i>, <i>365</i>(4), 522-526. <a href="https://doi.org/10.1002/adsc.202201408" target="_blank">https://doi.org/10.1002/adsc.202201408</a> | |
dc.identifier.other | CONVID_177039584 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/85660 | |
dc.description.abstract | Copper-catalyzed cross-coupling reactions of α-bromoaryl NH-sulfoximines with elemental sulfur lead to benzo[d][1,3,2]dithiazole-1-oxides, which represent a new class of three-dimensional heterocycles. The reactions proceed under mild conditions showing good functional group and heterocycle tolerance. By imination/oxidation, the initial cross-coupling products can be converted to unprecedented cyclic sulfonimidamides derivatives. Furthermore, a seven-membered heterocycle was obtained by a ruthenium-catalyzed ring-expansion with ethyl propiolate. | en |
dc.format.mimetype | application/pdf | |
dc.language.iso | eng | |
dc.publisher | Wiley | |
dc.relation.ispartofseries | Advanced Synthesis and Catalysis | |
dc.rights | CC BY 4.0 | |
dc.subject.other | copper catalysis | |
dc.subject.other | elemental sulfur | |
dc.subject.other | sulfoximines | |
dc.subject.other | sulfonimidamides | |
dc.subject.other | cross-coupling reactions | |
dc.title | Cyclic Sulfoximine and Sulfonimidamide Derivatives by Copper‐Catalyzed Cross‐Coupling Reactions with Elemental Sulfur | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-202302271922 | |
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.format.pagerange | 522-526 | |
dc.relation.issn | 1615-4150 | |
dc.relation.numberinseries | 4 | |
dc.relation.volume | 365 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2023 The Authors. Advanced Synthesis & Catalysis published by Wiley-VCH GmbH | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | katalyysi | |
dc.subject.yso | rikki | |
dc.subject.yso | kupari | |
dc.subject.yso | rikkiyhdisteet | |
dc.subject.yso | katalyytit | |
dc.subject.yso | heterosykliset yhdisteet | |
dc.subject.yso | kemiallinen synteesi | |
dc.format.content | fulltext | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8704 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p12305 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p19074 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p5731 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p15480 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p38837 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p8468 | |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.1002/adsc.202201408 | |
jyx.fundinginformation | P. W. is grateful to the China Scholarship Council (CSC) for a predoctoral stipend, and we acknowledge the Alexander von Humboldt Foundation for support of K. R. (AvH research award). Open Access funding enabled and organized by Projekt DEAL. | |
dc.type.okm | A1 | |