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New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions

Generation of hydrazoylketenes by thermal decomposition of N-(diphenylenamino)pyrrolediones is accompanied by 5-exo-trig ring closure to furnish a zwitterionic dihydropyrazolone species. In contrast to Lisowskaya's earlier report, we established that in most cycloaddition reactions such dihydro...

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Päätekijät: Rubin, M. A., Рубин, М. А.
Aineistotyyppi: Статья
Kieli:English
Julkaistu: Royal Society of Chemistry 2018
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Linkit:https://www.scopus.com/record/display.uri?eid=2-s2.0-84989244953&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=bdb9e675eb066253a25567c2e9fb420e&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28New+method+for%3a+In+situ+generation+of+enolate-iminium+1%2c4-dipoles+for+%5b4+%2b+2%5d+and+%5b4+%2b+1%5d+dipolar+heterocycloaddition+reactions%29&relpos=0&citeCnt=2&searchTerm=
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spelling ir-20.500.12258-34282020-07-31T10:07:43Z New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions Rubin, M. A. Рубин, М. А. Decomposition Cycloaddition Situ generation Cycloaddition reaction Generation of hydrazoylketenes by thermal decomposition of N-(diphenylenamino)pyrrolediones is accompanied by 5-exo-trig ring closure to furnish a zwitterionic dihydropyrazolone species. In contrast to Lisowskaya's earlier report, we established that in most cycloaddition reactions such dihydropyrazolones react as 1,4-dipoles. This reactivity pattern was demonstrated in several [4 + 4]-homodimerizations and in a series of [4 + 2] and [4 + 1] cycloaddition reactions with various dipolarophiles 2018-11-16T09:35:19Z 2018-11-16T09:35:19Z 2016 Статья Zhulanov, V.E., Dmitriev, M.V., Maslivets, A.N. , Rubin, M. New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions // RSC Advances. - Volume 6. - Issue 93. - Pages 90239-90247 https://www.scopus.com/record/display.uri?eid=2-s2.0-84989244953&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=bdb9e675eb066253a25567c2e9fb420e&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28New+method+for%3a+In+situ+generation+of+enolate-iminium+1%2c4-dipoles+for+%5b4+%2b+2%5d+and+%5b4+%2b+1%5d+dipolar+heterocycloaddition+reactions%29&relpos=0&citeCnt=2&searchTerm= http://hdl.handle.net/20.500.12258/3428 en RSC Advances application/pdf application/pdf Royal Society of Chemistry
institution СКФУ
collection Репозиторий
language English
topic Decomposition
Cycloaddition
Situ generation
Cycloaddition reaction
spellingShingle Decomposition
Cycloaddition
Situ generation
Cycloaddition reaction
Rubin, M. A.
Рубин, М. А.
New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
description Generation of hydrazoylketenes by thermal decomposition of N-(diphenylenamino)pyrrolediones is accompanied by 5-exo-trig ring closure to furnish a zwitterionic dihydropyrazolone species. In contrast to Lisowskaya's earlier report, we established that in most cycloaddition reactions such dihydropyrazolones react as 1,4-dipoles. This reactivity pattern was demonstrated in several [4 + 4]-homodimerizations and in a series of [4 + 2] and [4 + 1] cycloaddition reactions with various dipolarophiles
format Статья
author Rubin, M. A.
Рубин, М. А.
author_facet Rubin, M. A.
Рубин, М. А.
author_sort Rubin, M. A.
title New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
title_short New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
title_full New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
title_fullStr New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
title_full_unstemmed New method for: In situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
title_sort new method for: in situ generation of enolate-iminium 1,4-dipoles for [4 + 2] and [4 + 1] dipolar heterocycloaddition reactions
publisher Royal Society of Chemistry
publishDate 2018
url https://www.scopus.com/record/display.uri?eid=2-s2.0-84989244953&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=bdb9e675eb066253a25567c2e9fb420e&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28New+method+for%3a+In+situ+generation+of+enolate-iminium+1%2c4-dipoles+for+%5b4+%2b+2%5d+and+%5b4+%2b+1%5d+dipolar+heterocycloaddition+reactions%29&relpos=0&citeCnt=2&searchTerm=
https://dspace.ncfu.ru/handle/20.500.12258/3428
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