Show simple item record

dc.contributor.authorWang, Xianliang
dc.contributor.authorFrings, Marcus
dc.contributor.authorRissanen, Kari
dc.contributor.authorBolm, Carsten
dc.date.accessioned2024-02-21T11:51:31Z
dc.date.available2024-02-21T11:51:31Z
dc.date.issued2023
dc.identifier.citationWang, 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.otherCONVID_176551973
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/93547
dc.description.abstractN-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.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherAmerican Chemical Society (ACS)
dc.relation.ispartofseriesJournal of Organic Chemistry
dc.rightsIn Copyright
dc.subject.othercentral nervous system
dc.subject.otherchemical reactions
dc.subject.othergenetics
dc.subject.otherhydrocarbons
dc.subject.othersubstituents
dc.titleSynthesis of o-Sulfinylanilines from N-Alkyl Sulfoximines and Arynes
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202402212014
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.format.pagerange2666-2669
dc.relation.issn0022-3263
dc.relation.numberinseries4
dc.relation.volume88
dc.type.versionacceptedVersion
dc.rights.copyright© 2023 American Chemical Society
dc.rights.accesslevelopenAccessfi
dc.subject.ysohiilivedyt
dc.subject.ysoperinnöllisyystiede
dc.subject.ysokemialliset reaktiot
dc.subject.ysokeskushermosto
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p1169
jyx.subject.urihttp://www.yso.fi/onto/yso/p5147
jyx.subject.urihttp://www.yso.fi/onto/yso/p3658
jyx.subject.urihttp://www.yso.fi/onto/yso/p8647
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1021/acs.joc.3c00012
jyx.fundinginformationX.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.okmA1


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

In Copyright
Except where otherwise noted, this item's license is described as In Copyright