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Synthesis of 4-amino-1,3-diarylimidazolium chlorides Научная публикация

Журнал Doklady Chemistry
ISSN: 1608-3113 , E-ISSN: 0012-5008
Вых. Данные Год: 2024, Том: 515, Номер: 1, Страницы: 18-29 Страниц : 12 DOI: 10.31857/s2686953524020021
Авторы Shevchenko M.A. 1 , Pasyukov D.V. 1 , Lavrentiev I.V. 1 , Minyaev M.E. 2 , Chernyshev V.M. 1
Организации
1 Platov South-Russian State Polytechnic University (NPI)
2 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences

Реферат: The first representatives of 4-amino-1,3-diarylimidazolium chlorides have been synthesized by heating chloroacetonitrile with N,Nʹ-diarylformamidines containing alkyl substituents at positions 2 and 6 of the N-aryl groups. The possibility of postfunctionalization of the obtained aminoimidazolium salts by acylation of the amino group was demonstrated, as well as their applicability as precursors of N-heterocyclic carbenes in the synthesis of Cu/NHC complexes after preliminary protection of the amino group.
Библиографическая ссылка: Shevchenko M.A. , Pasyukov D.V. , Lavrentiev I.V. , Minyaev M.E. , Chernyshev V.M.
Synthesis of 4-amino-1,3-diarylimidazolium chlorides
Doklady Chemistry. 2024. V.515. N1. P.18-29. DOI: 10.31857/s2686953524020021 OpenAlex
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≡ OpenAlex: W4400410748
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