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Homocondensation of 1,3-di(5-acenaphthenyl)but-2-ene-1-one

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Abstract

Homocondensation of 1,3-di(5-acenaphthenyl)but-2-en-1-one obtained by dimerization of 5-acetylacenaphthene leads to 1,3,5-tri(5-acenaphthenyl)benzene. No alternative product, 1,3,5,7-tetra(5-acenaphthenyl)cyclooctatetraene, was formed.

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Correspondence to A. I. Kovalev.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 1994–1996, October, 2021.

This work was financially supported by the Russian Foundation for Basic Research (Project No. 20-03-00087). NMR studies were performed with the financial support from the Ministry of Science and Higher Education of the Russian Federation on the equipment of Center for Molecular Composition Studies of INEOS RAS.

This paper does not contain descriptions of studies on animals or humans.

The authors declare no competing interests.

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Kovalev, A.I., Khotina, I.A. Homocondensation of 1,3-di(5-acenaphthenyl)but-2-ene-1-one. Russ Chem Bull 70, 1994–1996 (2021). https://doi.org/10.1007/s11172-021-3307-z

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  • DOI: https://doi.org/10.1007/s11172-021-3307-z

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