Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/148218
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dc.contributor.authorHuang, Xiaoleien_US
dc.contributor.authorTeng, Shenghanen_US
dc.contributor.authorChi, Robin Yongguien_US
dc.contributor.authorXu, Wenqiangen_US
dc.contributor.authorPu, Maopingen_US
dc.contributor.authorWu, Yun-Dongen_US
dc.contributor.authorZhou, Steve Jianrongen_US
dc.date.accessioned2021-04-26T01:32:50Z-
dc.date.available2021-04-26T01:32:50Z-
dc.date.issued2021-
dc.identifier.citationHuang, X., Teng, S., Chi, R. Y., Xu, W., Pu, M., Wu, Y. & Zhou, S. J. (2021). Enantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickel. Angewandte Chemie International Edition, 60(6), 2828-2832. https://dx.doi.org/10.1002/anie.202011036en_US
dc.identifier.issn1521-3773en_US
dc.identifier.other0000-0001-7929-1987-
dc.identifier.other0000-0003-0573-257X-
dc.identifier.other0000-0003-4477-7332-
dc.identifier.other0000-0002-1806-7436-
dc.identifier.urihttps://hdl.handle.net/10356/148218-
dc.description.abstractNickel-catalyzed intermolecular Heck reaction of cycloalkenes proceeds well with aryl triflates, mesylates and tosylates in excellent enantiomeric ratios. The asymmetric reductive Heck reaction also works with a 2-cyclopentenone ketal, which is equivalent to conjugate arylation of the enone itself.en_US
dc.description.sponsorshipEconomic Development Board (EDB)en_US
dc.language.isoenen_US
dc.relation.ispartofAngewandte Chemie International Editionen_US
dc.rightsThis is the peer reviewed version of the following article: Huang, X., Teng, S., Chi, R. Y., Xu, W., Pu, M., Wu, Y. & Zhou, S. J. (2021). Enantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickel. Angewandte Chemie International Edition, 60(6), 2828-2832. https://dx.doi.org/10.1002/anie.202011036, which has been published in final form at https://doi.org/10.1002/anie.202011036. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.en_US
dc.subjectScienceen_US
dc.titleEnantioselective intermolecular Heck and reductive Heck reactions of aryl triflates, mesylates, and tosylates catalyzed by nickelen_US
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doi10.1002/anie.202011036-
dc.description.versionAccepted versionen_US
dc.identifier.pmid33140526-
dc.identifier.scopus2-s2.0-85097260623-
dc.identifier.issue6en_US
dc.identifier.volume60en_US
dc.identifier.spage2828en_US
dc.identifier.epage2832en_US
dc.subject.keywordsAryl Halidesen_US
dc.subject.keywordsHeck Reactionen_US
dc.description.acknowledgementWe acknowledge financial supports from Peking University Shenzhen Graduate School, Shenzhen Bay Laboratory Insti- tute of Chemical Biology, Nanyang Technological University, GlaxoSmithKline and the Singapore Economic Development Board Trust Fund (2017 GSK-EDB Green and Sustainable Manufacturing Award) and A*STAR Science and Engineer- ing Research Council (A1783c0010).en_US
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