ATTENTION: The software behind KU ScholarWorks is being upgraded to a new version. Starting July 15th, users will not be able to log in to the system, add items, nor make any changes until the new version is in place at the end of July. Searching for articles and opening files will continue to work while the system is being updated. If you have any questions, please contact Marianne Reed at mreed@ku.edu .

Show simple item record

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


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 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.