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Mendeleev Communications, 2007, Volume 17, Issue 2, Pages 116–118
DOI: https://doi.org/10.1016/j.mencom.2007.03.022
(Mi mendc3397)
 

This article is cited in 19 scientific papers (total in 19 papers)

Benzylamine imines as versatile precursors to azomethine and nitrile ylides in the [2 + 3] cycloaddition reactions with [60]fullerene

P. A. Troshina, A. B. Korneva, A. S. Peregudovb, S. M. Peregudovab, R. N. Lyubovskayaa

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
Abstract: Pyrrolidino- and pyrrolinofullerenes were prepared using readily available benzylamine imines as reagents; the cyclic voltammetry measurements revealed that the C=N double bond mediates an electronic communication between the fullerene π-system and a substituent attached to the sp2 carbon of the pyrroline ring.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (211.6 Kb)


Citation: P. A. Troshin, A. B. Kornev, A. S. Peregudov, S. M. Peregudova, R. N. Lyubovskaya, “Benzylamine imines as versatile precursors to azomethine and nitrile ylides in the [2 + 3] cycloaddition reactions with [60]fullerene”, Mendeleev Commun., 17:2 (2007), 116–118
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  • https://www.mathnet.ru/eng/mendc/v17/i2/p116
  • This publication is cited in the following 19 articles:
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