Synthesis of o-Sulfinylanilines from N-Alkyl Sulfoximines and Arynes
| dc.contributor.author | Wang, Xianliang | |
| dc.contributor.author | Frings, Marcus | |
| dc.contributor.author | Rissanen, Kari | |
| dc.contributor.author | Bolm, Carsten | |
| dc.date.accessioned | 2024-02-21T11:51:31Z | |
| dc.date.available | 2024-02-21T11:51:31Z | |
| dc.date.issued | 2023 | |
| dc.identifier.citation | Wang, X., Frings, M., Rissanen, K., & Bolm, C. (2023). Synthesis of o-Sulfinylanilines from N-Alkyl Sulfoximines and Arynes. <i>Journal of Organic Chemistry</i>, <i>88</i>(4), 2666-2669. <a href="https://doi.org/10.1021/acs.joc.3c00012" target="_blank">https://doi.org/10.1021/acs.joc.3c00012</a> | |
| dc.identifier.other | CONVID_176551973 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/93547 | |
| dc.description.abstract | N-Alkyl sulfoximines react with arynes generated in situ under mild conditions providing o-sulfinylanilines in good yields. The transformation is characterized by a broad substrate scope and a good functional group tolerance. The structure of a reaction product was confirmed by single-crystal X-ray diffraction. | en |
| dc.format.mimetype | application/pdf | |
| dc.language.iso | eng | |
| dc.publisher | American Chemical Society (ACS) | |
| dc.relation.ispartofseries | Journal of Organic Chemistry | |
| dc.rights | In Copyright | |
| dc.subject.other | central nervous system | |
| dc.subject.other | chemical reactions | |
| dc.subject.other | genetics | |
| dc.subject.other | hydrocarbons | |
| dc.subject.other | substituents | |
| dc.title | Synthesis of o-Sulfinylanilines from N-Alkyl Sulfoximines and Arynes | |
| dc.type | research article | |
| dc.identifier.urn | URN:NBN:fi:jyu-202402212014 | |
| 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 | 2666-2669 | |
| dc.relation.issn | 0022-3263 | |
| dc.relation.numberinseries | 4 | |
| dc.relation.volume | 88 | |
| dc.type.version | acceptedVersion | |
| dc.rights.copyright | © 2023 American Chemical Society | |
| dc.rights.accesslevel | openAccess | fi |
| dc.type.publication | article | |
| dc.subject.yso | hiilivedyt | |
| dc.subject.yso | perinnöllisyystiede | |
| dc.subject.yso | kemialliset reaktiot | |
| dc.subject.yso | keskushermosto | |
| dc.format.content | fulltext | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p1169 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p5147 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p3658 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p8647 | |
| dc.rights.url | http://rightsstatements.org/page/InC/1.0/?language=en | |
| dc.relation.doi | 10.1021/acs.joc.3c00012 | |
| jyx.fundinginformation | X.W. is grateful to the China Scholarship Council (CSC) for a predoctoral stipend, and the authors acknowledge the Alexander von Humboldt Foundation for support of K.R. (AvH research award). | |
| dc.type.okm | A1 |
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