Synthesis and X-ray diffraction analysis of coenzyme Q derivatives obtained from natural polyalkoxyallylbenzenes

A general synthetic access to methoxy analogues of coenzymes Q bearing functional substituents with various chain lengths at the quinone ring was developed using available natural (polymethoxy)(methylenedioxy)allylbenzenes. The Baeyer–Villiger rearrangement of (methylenedioxy)benzaldehydes into phenols followed by facile oxidation to quinones with the methylenedioxy moiety opening was identified as the key step in the synthesis of the target 1,4- and 1,2-polyalkoxyquinones © 2023

Авторы
Tsyganov D.V. , Demchuk D.V. , Adaeva O.I. , Konyushkin L.D. , Minyaev M.E. , Khrustalev V.N. , Semenov V.V.
Издательство
Royal Society of Chemistry
Номер выпуска
4
Язык
Английский
Страницы
539-542
Статус
Опубликовано
Том
33
Год
2023
Организации
  • 1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, 119991, Russian Federation
  • 2 Peoples Friendship University of Russia (RUDN University), Moscow, 117198, Russian Federation
Ключевые слова
(methylenedioxy)benzaldehyde; allylbenzenes; Baeyer–Villiger rearrangement; coenzyme Q; formylation; oxidation; polyalkoxyquinone
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Maharramov A., Shikhaliyev N.Q., Qajar A., Atakishiyeva G.T., Niyazova A., Khrustalev V.N., Akkurt M., Yildirim S.Ö., Bhattarai A.
Acta Crystallographica Section E: Crystallographic Communications. International Union of Crystallography. Том 79. 2023. С. 637-643