Bio-inspired domino reduction of nitroarenes by acrolein-amine conjugates in one-pot operation

dc.contributor.author	Takamatsu M.
dc.contributor.author	Fukase K.
dc.contributor.author	Tanaka K.
dc.date.accessioned	2018-09-19T20:32:35Z
dc.date.available	2018-09-19T20:32:35Z
dc.date.issued	2017
dc.identifier.issn	0366-7022
dc.identifier.uri	https://dspace.kpfu.ru/xmlui/handle/net/142997
dc.description.abstract	© 2017 The Chemical Society of Japan.Biologically relevant amines react with acrolein to provide 3-formyl-3,4-dehydropiperidine (FDP) as the oxidative stress product, which has reduction potential via hydrogen transfer. This biogenic process was applied to the domino reduction of electron-deficient nitroarenes in one-pot operation, by simply mixing primary amine, acrolein, nitroarene, and calcium chloride. The reaction can be performed in a gram-scale without the use of hazardous metals.
dc.relation.ispartofseries	Chemistry Letters
dc.subject	Bio-inspired domino reduction
dc.subject	FDP
dc.subject	Nitroarene
dc.title	Bio-inspired domino reduction of nitroarenes by acrolein-amine conjugates in one-pot operation
dc.type	Article
dc.relation.ispartofseries-issue	6
dc.relation.ispartofseries-volume	46
dc.collection	Публикации сотрудников КФУ
dc.relation.startpage	811
dc.source.id	SCOPUS03667022-2017-46-6-SID85020251850

Файлы в этом документе

Имя: SCOPUS03667022-20 ...

Размер: 46.58Kb

Формат: PDF

Публикации сотрудников КФУ Scopus [24551]
Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.