Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/86882
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dc.contributor.authorLei, Chuanhuen
dc.contributor.authorYip, Yong Jieen
dc.contributor.authorZhou, Jianrong Steveen
dc.date.accessioned2017-12-27T04:25:31Zen
dc.date.accessioned2019-12-06T16:30:52Z-
dc.date.available2017-12-27T04:25:31Zen
dc.date.available2019-12-06T16:30:52Z-
dc.date.issued2017en
dc.identifier.citationLei, C., Yip, Y. J., & Zhou, J. S. (2017). Nickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditions. Journal of the American Chemical Society, 139(17), 6086-6089.en
dc.identifier.issn0002-7863en
dc.identifier.urihttps://hdl.handle.net/10356/86882-
dc.description.abstractNickel-catalyzed addition of arylboron reagents to ketones results in aryl olefins directly. The neutral condition allows acidic protons of alcohols, phenols, and malonates to be present, and fragile structures are also tolerated.en
dc.description.sponsorshipMOE (Min. of Education, S’pore)en
dc.format.extent6 p.en
dc.language.isoenen
dc.relation.ispartofseriesJournal of the American Chemical Societyen
dc.rights© 2017 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Journal of the American Chemical Society, ACS Publications. 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/10.1021/jacs.7b02742].en
dc.subjectAryl Olefinsen
dc.subjectKetoneen
dc.titleNickel-Catalyzed Direct Synthesis of Aryl Olefins from Ketones and Organoboron Reagents under Neutral Conditionsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1021/jacs.7b02742en
dc.description.versionAccepted versionen
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