[6]–[9]Metacyclophanes › Обзор исследований

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[6]–[9]Metacyclophanes : Synthesis, Crystal Structures, and NMR and UV Spectroscopy. / Shuvalov, Vladislav Yu; Eltsov, Ilia V.; Tumanov, Nikolay A. и др.

в: European Journal of Organic Chemistry, Том 2017, № 36, 02.10.2017, стр. 5410-5416.

Результаты исследований: Научные публикации в периодических изданиях › статья › Рецензирование

Harvard

Shuvalov, VY, Eltsov, IV, Tumanov, NA, Boldyreva, EV , Nefedov, AA & Sagitullina, GP 2017, '[6]–[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy', European Journal of Organic Chemistry, Том. 2017, № 36, стр. 5410-5416. https://doi.org/10.1002/ejoc.201700946

APA

Shuvalov, V. Y., Eltsov, I. V., Tumanov, N. A., Boldyreva, E. V., Nefedov, A. A., & Sagitullina, G. P. (2017). [6]–[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy. European Journal of Organic Chemistry, 2017(36), 5410-5416. https://doi.org/10.1002/ejoc.201700946

Vancouver

Shuvalov VY, Eltsov IV, Tumanov NA, Boldyreva EV , Nefedov AA, Sagitullina GP. [6]–[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy. European Journal of Organic Chemistry. 2017 окт. 2;2017(36):5410-5416. doi: 10.1002/ejoc.201700946

Author

Shuvalov, Vladislav Yu ; Eltsov, Ilia V. ; Tumanov, Nikolay A. и др. / [6]–[9]Metacyclophanes : Synthesis, Crystal Structures, and NMR and UV Spectroscopy. в: European Journal of Organic Chemistry. 2017 ; Том 2017, № 36. стр. 5410-5416.

BibTeX

@article{cc491c83d2634dd1a93deedeff68606c,

title = "[6]–[9]Metacyclophanes: Synthesis, Crystal Structures, and NMR and UV Spectroscopy",

abstract = "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.",

keywords = "Aromaticity, Cyclophanes, N-Methylpyridinium salts, Nitropyridines, Rearrangement",

author = "Shuvalov, {Vladislav Yu} and Eltsov, {Ilia V.} and Tumanov, {Nikolay A.} and Boldyreva, {Elena V.} and Nefedov, {Andrey A.} and Sagitullina, {Galina P.}",

note = "Publisher Copyright: {\textcopyright} 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim",

year = "2017",

month = oct,

day = "2",

doi = "10.1002/ejoc.201700946",

language = "English",

volume = "2017",

pages = "5410--5416",

journal = "European Journal of Organic Chemistry",

issn = "1434-193X",

publisher = "Wiley-Blackwell",

number = "36",

}

RIS

TY - JOUR

T1 - [6]–[9]Metacyclophanes

T2 - Synthesis, Crystal Structures, and NMR and UV Spectroscopy

AU - Shuvalov, Vladislav Yu

AU - Eltsov, Ilia V.

AU - Tumanov, Nikolay A.

AU - Boldyreva, Elena V.

AU - Nefedov, Andrey A.

AU - Sagitullina, Galina P.

PY - 2017/10/2

Y1 - 2017/10/2

N2 - 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.

AB - 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.

KW - Aromaticity

KW - Cyclophanes

KW - N-Methylpyridinium salts

KW - Nitropyridines

KW - Rearrangement

UR - http://www.scopus.com/inward/record.url?scp=85030169118&partnerID=8YFLogxK

U2 - 10.1002/ejoc.201700946

DO - 10.1002/ejoc.201700946

M3 - Article

AN - SCOPUS:85030169118

VL - 2017

SP - 5410

EP - 5416

JO - European Journal of Organic Chemistry

JF - European Journal of Organic Chemistry

SN - 1434-193X

IS - 36

ER -

ID: 9032934