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dc.contributor.authorDudovtsev, Alexey Yu
dc.contributor.authorSilaichev, Pavel S.
dc.contributor.authorNazarov, Mikhail A.
dc.contributor.authorDmitriev, Maksim V.
dc.contributor.authorMaslivets, Andrey N.
dc.contributor.authorRubin, Michael
dc.date.accessioned2017-11-27T16:35:57Z
dc.date.available2017-11-27T16:35:57Z
dc.date.issued2016-09-02
dc.identifier.citationDubovtsev, A. Y., Silaichev, P. S., Nazarov, M. A., Dmitriev, M. V., Maslivets, A. N., & Rubin, M. (2016). Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines. RSC Advances, 6(88), 84730-84737. doi:10.1039/c6ra16889ben_US
dc.identifier.urihttp://hdl.handle.net/1808/25460
dc.description.abstractHighly efficient spiro-condensation enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed. The corresponding furo[3,2-c]coumarins and furo[3,2-c]quinolines containing a spiro pyrrole fragment were obtained in high yields.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.titleSpiro-condensation of 5-methoxycarbonyl-1Hpyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolinesen_US
dc.typeArticleen_US
kusw.kuauthorRubin, Michael
kusw.kudepartmentChemistryen_US
dc.identifier.doi10.1039/c6ra16889b
dc.identifier.orcidhttps://orcid.org/0000-0002-1668-9311
kusw.oaversionScholarly/refereed, publisher versionen_US
kusw.oapolicyThis item meets KU Open Access policy criteria.en_US
dc.rights.accessrightsopenAccessen_US


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This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
Except where otherwise noted, this item's license is described as: This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License 4.0 (CC BY-NC-ND 4.0), which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.