dc.contributor.authorGao, Ke
dc.contributor.authorPaira, Rupankar
dc.contributor.authorYoshikai, Naohiko
dc.date.accessioned2014-06-12T08:26:15Z
dc.date.available2014-06-12T08:26:15Z
dc.date.copyright2014en_US
dc.date.issued2014
dc.identifier.citationGao, K., Paira, R., & Yoshikai, N. (2014). Cobalt-Catalyzed ortho -C-H Alkylation of 2-Arylpyridines via Ring-Opening of Aziridines . Advanced Synthesis & Catalysis, 356(7), 1486-1490.en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://hdl.handle.net/10220/19713
dc.description.abstractA cobalt–N-heterocyclic carbene catalyst, in combination with neopentylmagnesium bromide, was found to promote ortho-C[BOND]H functionalization of 2-arylpyridines with 1,2-diarylaziridines through ring-opening alkylation. The reaction affords 1,1-diarylethanes bearing 2-amino functional groups in moderate to good yields under mild room-temperature conditions.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesAdvanced synthesis & catalysisen_US
dc.rights© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry
dc.titleCobalt-catalyzed ortho-C-H alkylation of 2-arylpyridines via ring-opening of aziridinesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1002/adsc.201400049


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