dc.contributor.author | Aksenov, Nicolai A. | |
dc.contributor.author | Aksenov, Dmitrii A. | |
dc.contributor.author | Arutiunov, Nikolai A. | |
dc.contributor.author | Aksenova, Daria S. | |
dc.contributor.author | Aksenov, Alexander V. | |
dc.contributor.author | Rubin, Michael | |
dc.date.accessioned | 2022-09-20T14:20:20Z | |
dc.date.available | 2022-09-20T14:20:20Z | |
dc.date.issued | 2020-05-14 | |
dc.identifier.citation | Aksenov, N.A.; et al. Unexpected cyclization of ortho-nitrochalcones into 2-alkylideneindolin-3-ones. RSC Adv., 2020,10, 18440-18450. https://doi.org/10.1039/D0RA03520C | en_US |
dc.identifier.uri | http://hdl.handle.net/1808/33539 | |
dc.description.abstract | An original, facile, and highly efficient method for the preparation of 2-(3-oxoindolin-2-ylidene)acetonitriles from ortho-nitrochalcones is described. The featured transformation is a triggered Michael addition of the cyanide anion to the chalcone followed by a cascade cyclization mechanistically related to the Baeyer–Drewson reaction. | 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 | Unexpected cyclization of ortho-nitrochalcones into 2-alkylideneindolin-3-ones | en_US |
dc.type | Article | en_US |
kusw.kuauthor | Rubin, Michael | |
kusw.kudepartment | Chemistry | en_US |
dc.identifier.doi | 10.1039/D0RA03520C | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-7125-9066 | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-0727-9652 | 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 |