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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 (Данные Web of science) FM Dostoevsky Omsk State Univ, Dept Organ Chem, Omsk 644077, Russia
2 (Данные Web of science) Novosibirsk State Univ, Novosibirsk 630090, Russia
3 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia
4 (Данные Web of science) Univ Namur, Dept Chem, Rue Bruxelles 61, B-5000 Namur, Belgium

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.
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 OpenAlex
Даты:
Опубликована online: 29 сент. 2017 г.
Опубликована в печати: 2 окт. 2017 г.
Идентификаторы БД:
Web of science: WOS:000412127100006
Scopus: 2-s2.0-85030169118
РИНЦ: 31051478
OpenAlex: W2742255552
Цитирование в БД:
БД Цитирований
Web of science 3
Scopus 3
РИНЦ 5
OpenAlex 3
Альметрики: