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[6]-[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy Научная публикация

Журнал European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690
Вых. Данные Год: 2017, Том: 2017, Номер: 36, Страницы: 5410-5416 Страниц : 7 DOI: 10.1002/ejoc.201700946
Ключевые слова Aromaticity, Cyclophanes, N-Methylpyridinium salts, Nitropyridines, Rearrangement
Авторы Shuvalov Vladislav Yu. 1 , Eltsov Ilia V. 2 , Tumanov Nikolay A. 2,4 , Boldyreva Elena V. 2 , Nefedov Andrey A. 3 , Sagitullina Galina P. 1
Организации
1 Department of Organic Chemistry, F. M. Dostoevsky Omsk State University, 644077 Omsk, Russian Federation
2 Novosibirsk State University, 630090 Novosibirsk, Russian Federation
3 N. N. Vorozhtsov Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences
4 Department of Chemistry, University of Namur, rue de Bruxelles 61, 5000 Namur, Belgium

Информация о финансировании (1)

1 Российский фонд фундаментальных исследований 16-43-550144 (АААА-А16-116040810158-3)

Реферат: Metacyclophanes have been developed as non-planar aromatic compounds with unusual physical properties. [6]–[9]Metacyclophanes were synthesized by rearrangement of 3-nitro(perhydrocycloalka)[b]pyridinium salts, and analysis of their spectroscopic data and X-ray diffraction patterns indicates the aromaticity and flexibility of their benzene rings. The effectiveness and simplicity of the synthesis makes it possible to use them as available precursors in the synthesis of retinoids, indolophanes, and carbazolophanes. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Библиографическая ссылка: Shuvalov V.Y. , Eltsov I.V. , Tumanov N.A. , Boldyreva E.V. , Nefedov A.A. , Sagitullina G.P.
[6]-[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy
European Journal of Organic Chemistry. 2017. V.2017. N36. P.5410-5416. DOI: 10.1002/ejoc.201700946 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 7 июл. 2017 г.
Опубликована online: 11 авг. 2017 г.
Опубликована в печати: 2 окт. 2017 г.
Идентификаторы БД:
Web of science: WOS:000412127100006
Scopus: 2-s2.0-85030169118
РИНЦ: 31051478
Chemical Abstracts: 2017:1577113
Chemical Abstracts (print): 167:495881
OpenAlex: W2742255552
Цитирование в БД:
БД Цитирований
Web of science 3
Scopus 3
OpenAlex 3
Альметрики: