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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2023, том 33, выпуск 6, страницы 774–775 (Mi mendc520)

Эта публикация цитируется в 1 статье

Communications

Synthesis of a new apiol-derived cyclotriveratrylene analog

A. V. Samet, D. V. Tsyganov, V. P. Kislyi, E. I. Tujarov, V. V. Semenov

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation


Аннотация: 1,4,6,9,11,14-Hexamethoxy-2,3,7,8,12,13-tris(methylene-dioxy)-10,15-dihydro-5H-tribenzo[a,d,g][9] annulene, a new representative of a cyclotriveratrylene family, was prepared in high yield by acid-catalyzed trimerization of 2,5-di-methoxy-3,4-(methylenedioxy)benzyl alcohol. Structure of the product was confirmed by X-ray diffraction.

Ключевые слова: cyclotriveratrylene, molecular hosts, tribenzo[a,d,g][9]annulenes, apiol, 2,5-dimethoxy-3,4-(methylenedioxy)benzyl alcohol, trimerization.

Язык публикации: английский

DOI: 10.1016/j.mencom.2023.10.011



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