[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.
| Main Authors: | , , , , , , , , , |
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| Format: | Article |
| Language: | English |
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The Royal Society
2022-03-01
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| Series: | Royal Society Open Science |
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| Online Access: | https://royalsocietypublishing.org/doi/10.1098/rsos.211967 |
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| author | Maxim E. Kukushkin Alexandra A. Kondratieva Nikita A. Karpov Dmitry E. Shybanov Viktor A. Tafeenko Vitaly A. Roznyatovsky Yuri K. Grishin Anna A. Moiseeva Nikolai V. Zyk Elena K. Beloglazkina |
| author_facet | Maxim E. Kukushkin Alexandra A. Kondratieva Nikita A. Karpov Dmitry E. Shybanov Viktor A. Tafeenko Vitaly A. Roznyatovsky Yuri K. Grishin Anna A. Moiseeva Nikolai V. Zyk Elena K. Beloglazkina |
| author_sort | Maxim E. Kukushkin |
| collection | DOAJ |
| 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. |
| first_indexed | 2024-04-09T15:27:57Z |
| format | Article |
| id | doaj.art-73126e35fd154a94955547ab1a4839b5 |
| institution | Directory Open Access Journal |
| issn | 2054-5703 |
| language | English |
| last_indexed | 2024-04-09T15:27:57Z |
| publishDate | 2022-03-01 |
| publisher | The Royal Society |
| record_format | Article |
| series | Royal Society Open Science |
| spelling | doaj.art-73126e35fd154a94955547ab1a4839b52023-04-28T11:04:59ZengThe Royal SocietyRoyal Society Open Science2054-57032022-03-019310.1098/rsos.211967[3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolonesMaxim E. Kukushkin0Alexandra A. Kondratieva1Nikita A. Karpov2Dmitry E. Shybanov3Viktor A. Tafeenko4Vitaly A. Roznyatovsky5Yuri K. Grishin6Anna A. Moiseeva7Nikolai V. Zyk8Elena K. Beloglazkina9Department of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationDepartment of Chemistry, M.V. Lomonosov Moscow State University, Leninskie Gory, 1-3, 119991 Moscow, Russian FederationA synthesis of dispiro derivatives from 5-methylidene-2-chalcogenimidazolones and azomethine ylides generated from isatins and N-substituted α-amino acids has been developed.https://royalsocietypublishing.org/doi/10.1098/rsos.211967dispiro derivatives1,3-dipolar cycloadditionazomethine ylides5-methylidene-2-chalcogen-imidazolones |
| spellingShingle | Maxim E. Kukushkin Alexandra A. Kondratieva Nikita A. Karpov Dmitry E. Shybanov Viktor A. Tafeenko Vitaly A. Roznyatovsky Yuri K. Grishin Anna A. Moiseeva Nikolai V. Zyk Elena K. Beloglazkina [3+2]-Cycloaddition of azomethine ylides to 5-methylidene-3-aryl-2-сhalcogen-imidazolones: access to dispiro indolinone-pyrrolidine-imidazolones Royal Society Open Science dispiro derivatives 1,3-dipolar cycloaddition azomethine ylides 5-methylidene-2-chalcogen-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 | dispiro derivatives 1,3-dipolar cycloaddition azomethine ylides 5-methylidene-2-chalcogen-imidazolones |
| url | https://royalsocietypublishing.org/doi/10.1098/rsos.211967 |
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