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[3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones
A synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substituted α-amino acids has been developed.
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Royal Society
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905182/ https://www.ncbi.nlm.nih.gov/pubmed/35291328 http://dx.doi.org/10.1098/rsos.211967 |
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| author | Kukushkin, Maxim E. Kondratieva, Alexandra A. Karpov, Nikita A. Shybanov, Dmitry E. Tafeenko, Viktor A. Roznyatovsky, Vitaly A. Grishin, Yuri K. Moiseeva, Anna A. Zyk, Nikolai V. Beloglazkina, Elena K. |
| author_facet | Kukushkin, Maxim E. Kondratieva, Alexandra A. Karpov, Nikita A. Shybanov, Dmitry E. Tafeenko, Viktor A. Roznyatovsky, Vitaly A. Grishin, Yuri K. Moiseeva, Anna A. Zyk, Nikolai V. Beloglazkina, Elena K. |
| author_sort | Kukushkin, Maxim E. |
| collection | PubMed |
| description | A synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substituted α-amino acids has been developed. |
| format | Online Article Text |
| id | pubmed-8905182 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2022 |
| publisher | The Royal Society |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-89051822022-03-14 [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones Kukushkin, Maxim E. Kondratieva, Alexandra A. Karpov, Nikita A. Shybanov, Dmitry E. Tafeenko, Viktor A. Roznyatovsky, Vitaly A. Grishin, Yuri K. Moiseeva, Anna A. Zyk, Nikolai V. Beloglazkina, Elena K. R Soc Open Sci Chemistry A synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substituted α-amino acids has been developed. The Royal Society 2022-03-09 /pmc/articles/PMC8905182/ /pubmed/35291328 http://dx.doi.org/10.1098/rsos.211967 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
| spellingShingle | Chemistry Kukushkin, Maxim E. Kondratieva, Alexandra A. Karpov, Nikita A. Shybanov, Dmitry E. Tafeenko, Viktor A. Roznyatovsky, Vitaly A. Grishin, Yuri K. Moiseeva, Anna A. Zyk, Nikolai V. Beloglazkina, Elena K. [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title | [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title_full | [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title_fullStr | [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title_full_unstemmed | [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title_short | [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| title_sort | [3+2]-cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones |
| topic | Chemistry |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8905182/ https://www.ncbi.nlm.nih.gov/pubmed/35291328 http://dx.doi.org/10.1098/rsos.211967 |
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