Palladium-Catalyzed Access to Benzocyclobutenone-Derived Ketonitrones via C(sp2)–H Functionalization
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dc.contributor.author | Brześkiewicz, Jakub | |
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dc.contributor.author | Loska, Rafał | |
dc.contributor.organization | Institute of Organic Chemistry, Polish Academy of Sciences | en |
dc.date.accessioned | 2022-10-21T13:54:18Z | |
dc.date.available | 2022-10-21T13:54:18Z | |
dc.date.issued | 2022 | |
dc.description.abstract | The palladium-catalyzed C(sp2)–H functionalization of bromoaryl aldonitrones leading to benzocyclobutenone-derived ketonitrones is described. This method allows for the preparation of a wide range of strained, four-membered ketonitrones with broad functional group tolerance. Downstream transformations of the formed products were readily demonstrated, illustrating the synthetic utility of the obtained benzocyclobutenone-derived nitrones for the construction of polycyclic nitrogen-containing scaffolds. | en |
dc.description.sponsorship | National Science Centre SONATA BIS 7 Grant (UMO-2017/26/E/ST5/00388); National Science Centre PRELUDIUM 19 Grant (Grant UMO-2020/37/N/ST4/00777); Ministry of Science and Education, Poland, DIAMENTOWY GRANT VIII Program (Grant 0235/DIA/2019/48) | |
dc.identifier.citation | Org. Lett. 2022, 24, 22, 3960–3964 ; https://doi.org/10.1021/acs.orglett.2c01317 | en |
dc.identifier.doi | 10.1021/acs.orglett.2c01317 | |
dc.identifier.issn | 1523-7060 | |
dc.identifier.issn | 1523-7052 | |
dc.identifier.uri | https://open.icm.edu.pl/handle/123456789/21767 | |
dc.language.iso | en | |
dc.publisher | American Chemical Society | en |
dc.rights | Uznanie autorstwa 4.0 Międzynarodowe | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject | aAromatic compounds | en |
dc.subject | cyclization | en |
dc.subject | functionalization | en |
dc.subject | hydrocarbons | en |
dc.subject | nitrogen compounds | en |
dc.title | Palladium-Catalyzed Access to Benzocyclobutenone-Derived Ketonitrones via C(sp2)–H Functionalization | en |
dc.type | article | en |
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