A. V. Samet, D. V. Tsyganov, V. P. Kislyi, E. I. Tujarov, V. V. Semenov, “Synthesis of a new apiol-derived cyclotriveratrylene analog”, Mendeleev Commun., 33:6 (2023), 774

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Mendeleev Communications, 2023, Volume 33, Issue 6, Pages 774–775
DOI: https://doi.org/10.1016/j.mencom.2023.10.011 (Mi mendc520)

This article is cited in 2 scientific papers (total in 2 papers)

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

Full-text PDF (467 kB) Citations (2)

DOI: https://doi.org/10.1016/j.mencom.2023.10.011

Graphic abstract: Synthesis of a new apiol-derived cyclotriveratrylene analog

Abstract: 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.

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

Document Type: Article

Language: English

*Supplementary materials:*
		Supplementary_data_1.pdf	(305.9 Kb)

Citation: A. V. Samet, D. V. Tsyganov, V. P. Kislyi, E. I. Tujarov, V. V. Semenov, “Synthesis of a new apiol-derived cyclotriveratrylene analog”, Mendeleev Commun., 33:6 (2023), 774–775

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https://www.mathnet.ru/eng/mendc/v33/i6/p774

This publication is cited in the following 2 articles:

Citing articles in Google Scholar: Russian citations, English citations
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