Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids

dc.citation.firstpage10018en_US
dc.citation.issueNumber33en_US
dc.citation.journalTitleAngewandte Chemieen_US
dc.citation.lastpage10022en_US
dc.citation.volumeNumber129en_US
dc.contributor.authorMa, Zhiweien_US
dc.contributor.authorZhou, Zheen_US
dc.contributor.authorKürti, Lászlóen_US
dc.date.accessioned2017-11-14T18:08:23Zen_US
dc.date.available2017-11-14T18:08:23Zen_US
dc.date.issued2017en_US
dc.description.abstractA RhII-catalyzed direct and stereospecific N-H- and N-alkyl aziridination of olefins is reported that uses hydroxylamine-O-sulfonic acids as inexpensive, readily available, and nitro group-free aminating reagents. Unactivated olefins, featuring a wide range of functional groups, are converted into the corresponding N-H or N-alkyl aziridines in good to excellent yields. This operationally simple, scalable transformation proceeds efficiently at ambient temperature and is tolerant towards oxygen and trace moisture.en_US
dc.identifier.citationMa, Zhiwei, Zhou, Zhe and Kürti, László. "Direct and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acids." <i>Angewandte Chemie,</i> 129, no. 33 (2017) Wiley: 10018-10022. https://doi.org/10.1002/ange.201705530.en_US
dc.identifier.digitalFINAL_Angewandte_HOSA_May_30_2017_Zhiwei_ZZ_Kurti-1en_US
dc.identifier.doihttps://doi.org/10.1002/ange.201705530en_US
dc.identifier.urihttps://hdl.handle.net/1911/98799en_US
dc.language.isoengen_US
dc.publisherWileyen_US
dc.rightsThis is an author's peer-reviewed final manuscript, as accepted by the publisher. The published article is copyrighted by Wiley.en_US
dc.subject.keywordaziridinationen_US
dc.subject.keyworddirhodium catalysisen_US
dc.subject.keywordhydroxylamine-O-sulfonic aciden_US
dc.subject.keywordnitrenoidsen_US
dc.subject.keywordolefinsen_US
dc.titleDirect and Stereospecific Synthesis of N-H and N-Alkyl Aziridines from Unactivated Olefins Using Hydroxylamine-O-Sulfonic Acidsen_US
dc.typeJournal articleen_US
dc.type.dcmiTexten_US
dc.type.publicationpost-printen_US
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