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Spiro-condensation of 5-methoxycarbonyl-1Hpyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines
dc.contributor.author | Dudovtsev, Alexey Yu | |
dc.contributor.author | Silaichev, Pavel S. | |
dc.contributor.author | Nazarov, Mikhail A. | |
dc.contributor.author | Dmitriev, Maksim V. | |
dc.contributor.author | Maslivets, Andrey N. | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2017-11-27T16:35:57Z | |
dc.date.available | 2017-11-27T16:35:57Z | |
dc.date.issued | 2016-09-02 | |
dc.identifier.citation | Dubovtsev, 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/c6ra16889b | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/25460 | |
dc.description.abstract | Highly 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.publisher | Royal Society of Chemistry | en_US |
dc.rights | 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. | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | en_US |
dc.title | Spiro-condensation of 5-methoxycarbonyl-1Hpyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1039/c6ra16889b | |
dc.identifier.orcid | https://orcid.org/0000-0002-1668-9311 | |
kusw.oaversion | Scholarly/refereed, publisher version | en_US |
kusw.oapolicy | This item meets KU Open Access policy criteria. | en_US |
dc.rights.accessrights | openAccess | en_US |
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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.