New Tetracyclic Spiro-1,2,4-trioxolanes (Ozonides). Synthesis and Mass Spectrometric Study


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New tetracyclic dispiro-1,2,4-trioxolanes (ozonides) were synthesized by reactions of 5–7-membered alicyclic 1,5-diketones with 30% hydrogen peroxide in diethyl ether or ethanol in the presence of boron trifluoride-diethyl ether complex or a strong mineral acid (HCl, H2SO4, HClO4). Mass spectrometric study of the title compounds under atmospheric pressure chemical ionization revealed specificity of fragment ion decomposition with respect to the ring size, which makes it possible to identify such compounds by their mass spectra.

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T. Akimova

Far Eastern Federal University

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Email: akimova.ti@dvfu.ru
俄罗斯联邦, ul. Sukhanova 8, Vladivostok, 690091

V. Rybin

Zhirmunskii Institute of Marine Biology, Far Eastern Branch

Email: akimova.ti@dvfu.ru
俄罗斯联邦, ul. Pal’chevskogo 17, Vladivostok, 690041

O. Soldatkina

Far Eastern Federal University

Email: akimova.ti@dvfu.ru
俄罗斯联邦, ul. Sukhanova 8, Vladivostok, 690091

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