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dc.contributor.authorGu, Xingxian
dc.contributor.authorGeorg, Gunda I.
dc.date.accessioned2021-10-05T20:33:18Z
dc.date.available2021-10-05T20:33:18Z
dc.date.issued2013-09-05
dc.identifier.citationGu, X., & Georg, G. I. (2013). Lithium Perchlorate-, Acetic Anhydride-, and Triphenylphosphine-assisted Multicomponent Syntheses of 4-Unsubstituted 2,5-Dioxooctahydroquinoline-3-carboxylates and 3-carbonitriles. Tetrahedron, 69(45), 9406–9416. doi:10.1016/j.tet.2013.08.081en_US
dc.identifier.urihttp://hdl.handle.net/1808/31911
dc.description.abstractLithium perchlorate and acetic anhydride were the key additives for the multi-component reaction between 3-aminocyclohex-2-enones, formaldehyde, and malonates yielding adducts that were annulated under acidic conditions to afford bicyclic 2,5-dioxooctahydroquinoline-3-carboxylates. When methyl cyanoacetate was subjected to the same reaction conditions in the presence of a catalytic amount of triphenylphosphine, the bicyclic 2,5-dioxooctahydroquinoline-3-carbonitriles were obtained in a one-flask reaction.en_US
dc.publisherElsevieren_US
dc.rights© 2013 Elsevier Ltd. This work is licensed under a Creative Commons Attribution Non-Commercial-No Derivatives 4.0 International License.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.titleLithium perchlorate-, acetic anhydride-, and triphenylphosphine-assisted multicomponent syntheses of 4-unsubstituted 2,5-dioxooctahydroquinoline-3-carboxylates and 3-carbonitrilesen_US
dc.typeArticleen_US
kusw.kuauthorGu, Xingxian
kusw.kudepartmentDepartment of Medicinal Chemistryen_US
dc.identifier.doi10.1016/j.tet.2013.08.081en_US
kusw.oaversionScholarly/refereed, author accepted manuscripten_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.identifier.pmidPMC6884338en_US
dc.rights.accessrightsopenAccessen_US


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© 2013 Elsevier Ltd.  This work is licensed under a Creative Commons Attribution Non-Commercial-No Derivatives 4.0 International License.
Except where otherwise noted, this item's license is described as: © 2013 Elsevier Ltd. This work is licensed under a Creative Commons Attribution Non-Commercial-No Derivatives 4.0 International License.