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dc.contributor.authorCartwright, Kaitie C.
dc.contributor.authorTunge, Jon A.
dc.date.accessioned2021-12-22T20:35:57Z
dc.date.available2021-12-22T20:35:57Z
dc.date.issued2020-07-16
dc.identifier.citationCartwright, K. C., & Tunge, J. A. (2020). Organophotoredox/palladium dual catalytic decarboxylative Csp3-Csp3 coupling of carboxylic acids and π-electrophiles. Chemical science, 11(31), 8167–8175. https://doi.org/10.1039/d0sc02609cen_US
dc.identifier.urihttp://hdl.handle.net/1808/32306
dc.description.abstractA dual catalytic decarboxylative allylation and benzylation method for the construction of new C(sp3)–C(sp3) bonds between readily available carboxylic acids and functionally diverse carbonate electrophiles has been developed. The new process is mild, operationally simple, and has greatly improved upon the efficiency and generality of previous methodology. In addition, new insights into the reaction mechanism have been realized and provide further understanding of the harnessed reactivity.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© The Royal Society of Chemistry 2020. This work is licensed under a Creative Commons Attribution 4.0 International License.en_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.titleOrganophotoredox/palladium dual catalytic decarboxylative Csp3–Csp3 coupling of carboxylic acids and π-electrophilesen_US
dc.typeArticleen_US
kusw.kuauthorCartwright, Kaitie C.
kusw.kuauthorTunge, Jon A.
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/d0sc02609cen_US
dc.identifier.orcidhttps://orcid.org/ 0000-0002-5849-0888en_US
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC8163213en_US
dc.rights.accessrightsopenAccessen_US


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© The Royal Society of Chemistry 2020. This work is licensed under a Creative Commons Attribution 4.0 International License.
Except where otherwise noted, this item's license is described as: © The Royal Society of Chemistry 2020. This work is licensed under a Creative Commons Attribution 4.0 International License.