dc.contributor.authorYamakawa, Takeshi
dc.contributor.authorSeto, Yuan Wah
dc.contributor.authorYoshikai, Naohiko
dc.date.accessioned2015-02-18T01:53:03Z
dc.date.available2015-02-18T01:53:03Z
dc.date.copyright2015en_US
dc.date.issued2015
dc.identifier.citationYamakawa, T., Seto, Y. W., & Yoshikai, N. (2015). Cobalt-catalyzed directed alkylation of olefinic C-H bond with primary and secondary alkyl chlorides. Synlett, 26(03), 340-344.en_US
dc.identifier.citation5 p.en_US
dc.identifier.urihttp://hdl.handle.net/10220/25072
dc.description.abstractA cobalt–N-heterocyclic carbene catalytic system promotes pyridine-directed olefinic C–H alkylation reactions using a variety of primary and secondary alkyl chlorides under mild conditions. Radical clock experiments suggest that the reaction involves single-electron transfer from the cobalt intermediate to the alkyl chloride.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesSynletten_US
dc.rights© 2015 Georg Thieme Verlag Stuttgart · New York. This is the author created version of a work that has been peer reviewed and accepted for publication by Synlett, Georg Thieme Verlag Stuttgart · New York. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1055/s-0034-1379247].en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry
dc.titleCobalt-catalyzed directed alkylation of olefinic C-H bond with primary and secondary alkyl chloridesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1055/s-0034-1379247
dc.description.versionAccepted versionen_US


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