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Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines
dc.contributor.author | Shcherbakov, Stanislav S. | |
dc.contributor.author | Magometov, Artyom Yu. | |
dc.contributor.author | Shcherbakova, Viktoriia Yu. | |
dc.contributor.author | Aksenov, Alexander V. | |
dc.contributor.author | Domenyuk, Dmitriy A. | |
dc.contributor.author | Zelensky, Vladimir A. | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2022-09-20T14:10:07Z | |
dc.date.available | 2022-09-20T14:10:07Z | |
dc.date.issued | 2020-03-10 | |
dc.identifier.citation | Shcherbakov, S.S.; et al. Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines. RSC Adv., 2020,10, 10315-10321. https://doi.org/10.1039/D0RA01335H | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/33538 | |
dc.description.abstract | A new synthetic protocol for preparation of medicinally important 4-aryl-5-alkynylpyrimidines is described. The featured approach involves a sequence of chemo- and regioselective Brønsted acid-catalyzed electrophilic alkylation of arenes with 5-bromopyrimidine, followed by oxidative re-aromatization of the formed dihydropyrimidine ring. Finally, palladium-catalyzed Sonogashira cross-coupling reaction provided an end-game strategy. | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.rights | © The Royal Society of Chemistry 2020. This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/3.0/ | en_US |
dc.title | Electrophilic alkylation of arenes with 5-bromopyrimidine en route to 4-aryl-5-alkynylpyrimidines | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1039/D0RA01335H | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-6644-9949 | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-1668-9311 | en_US |
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 |