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Alkyl-1,4-Benzoquinones - From Synthesis to Application Обзор

Журнал ChemistrySelect
, E-ISSN: 2365-6549
Вых. Данные Год: 2016, Том: 1, Номер: 10, Страницы: 2113-2128 Страниц : 16 DOI: 10.1002/slct.201600148, 10.1002/chin.201651263
Ключевые слова alkyl-1,4-benzoquinones, catalysis, environmental chemistry, oxidation, substituted phenols
Авторы Rodikova Yulia A. 1 , Zhizhina Elena G. 1 , Pai Zinaida P. 1
Организации
1 Department of Catalytic Processes of Fine Organic and Bioorganic Synthesis, Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russian Federation

Информация о финансировании (1)

1 Федеральное агентство научных организаций России V.44.2.8.

Реферат: Alkyl-1,4-benzoquinones (ABQs) such as 2,3-, 2,5- and 2,6-dimethyl- and 2,6-di-tert-butyl-1,4-benzoquinones are versatile building blocks and also have many others applications known for this type of compounds. Nowadays the requirements of environmental safety necessitate revising preparation processes of such compounds and searching for alternative synthesis ways. Until recently, there have been many efforts to develop sustainable green processes. However, the efficiency of proposed methods differs significantly. For this reason, in this review we would like to outline a variety of chemical properties of ABQs in order to show their great potential as chemical precursors, to describe some interesting applications of ABQs and then to give description of existing ABQ synthesis procedures developed in the last few decades. The review summarizes advances in liquid-phase selective oxidation of alkylphenols with molecular oxygen, hydrogen peroxide, and t-butyl hydroperoxide by using both homogeneous and heterogeneous catalysts. Consideration of old methods for ABQ synthesis is of interest for understanding the evolution of preferences in the field and for comparing the efficiency of methods.
Библиографическая ссылка: Rodikova Y.A. , Zhizhina E.G. , Pai Z.P.
Alkyl-1,4-Benzoquinones - From Synthesis to Application
ChemistrySelect. 2016. V.1. N10. P.2113-2128. DOI: 10.1002/slct.201600148, 10.1002/chin.201651263 WOS Scopus РИНЦ CAPlusCA OpenAlex
Даты:
Поступила в редакцию: 25 февр. 2016 г.
Принята к публикации: 30 мая 2016 г.
Опубликована в печати: 1 июл. 2016 г.
Опубликована online: 4 июл. 2016 г.
Идентификаторы БД:
Web of science: WOS:000395417800005
Scopus: 2-s2.0-85031278219
РИНЦ: 35504997
Chemical Abstracts: 2016:1614271
Chemical Abstracts (print): 165:487427
OpenAlex: W2470838654
Цитирование в БД:
БД Цитирований
Web of science 11
Scopus 11
OpenAlex 10
Альметрики: