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

Authors
Tsyganov D.V. , Demchuk D.V. , Adaeva O.I. , Konyushkin L.D. , Minyaev M.E. , Khrustalev V.N. , Semenov V.V.
Publisher
Royal Society of Chemistry
Issue number
4
Language
English
Pages
539-542
State
Published
Volume
33
Year
2023
Organizations
  • 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
Keywords
(methylenedioxy)benzaldehyde; allylbenzenes; Baeyer–Villiger rearrangement; coenzyme Q; formylation; oxidation; polyalkoxyquinone
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