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 |
|