Synthesis of a new apiol-derived cyclotriveratrylene analog Full article
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Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436 |
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| Output data | Year: 2023, Volume: 33, Number: 6, Pages: 774-775 Pages count : 2 DOI: 10.1016/j.mencom.2023.10.011 | ||
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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.
Cite:
Samet A.V.
, Tsyganov D.V.
, Kislyi V.P.
, Tujarov E.I.
, Semenov V.V.
Synthesis of a new apiol-derived cyclotriveratrylene analog
Mendeleev Communications. 2023. V.33. N6. P.774-775. DOI: 10.1016/j.mencom.2023.10.011 WOS Scopus OpenAlex
Synthesis of a new apiol-derived cyclotriveratrylene analog
Mendeleev Communications. 2023. V.33. N6. P.774-775. DOI: 10.1016/j.mencom.2023.10.011 WOS Scopus OpenAlex
Identifiers:
| Web of science: | WOS:001128215400001 |
| Scopus: | 2-s2.0-85179047160 |
| OpenAlex: | W4389121261 |