Synthesis of Polyalkoxymethylenedioxy-1,4-naphthoquinones from Parsley Seed Metabolite

A convenient synthesis of polyalkoxy-1,4-naphthoquinones, good starting materials for analogues of natural quinones, has been developed. Bromonaphthoquinone, more stable than its hydroxylated analogue, turned out to be a convenient and accessible key synthon for the preparation of various polyalkoxylated naphthoquinones. The obtained quinones could be useful starting materials for the preparation of biologically active polymethoxy- and hydroxy-methylenedioxynaphthoquinones.

Авторы
Varakutin A.E. 1 , Muravsky E.A. 1 , Khrustalev V.N. 1, 2 , Samet A.V. 1 , Semenov V.V. 1
Издательство
BENTHAM SCIENCE PUBL LTD
Номер выпуска
1
Язык
English
Страницы
40-45
Статус
Published
Том
28
Год
2024
Организации
  • 1 RAS, Lab Med Chem, ND Zelinsky Inst Organ Chem, 47 Leninsky Prospect, Moscow 119991, Russia
  • 2 RUDN Univ, Dept Organ Chem, 6 Miklukho Maklay St, Moscow 117198, Russia
Ключевые слова
Parsley; apiol; polyalkoxy-1,4-naphthoquinones; antioxidant; dioxolane ring; natural quinones
Цитировать
Поделиться

Другие записи

Avatkov V.A., Apanovich M.Yu., Borzova A.Yu., Bordachev T.V., Vinokurov V.I., Volokhov V.I., Vorobev S.V., Gumensky A.V., Иванченко В.С., Kashirina T.V., Матвеев О.В., Okunev I.Yu., Popleteeva G.A., Sapronova M.A., Свешникова Ю.В., Fenenko A.V., Feofanov K.A., Tsvetov P.Yu., Shkolyarskaya T.I., Shtol V.V. ...
Общество с ограниченной ответственностью Издательско-торговая корпорация "Дашков и К". 2018. 411 с.