Redox Amination Scope of Benzylic Ketones with Indoline: Synthetic and Mechanistic Insights

dc.contributor.author	Aydin, O. and Kilic, H. and Bayindir, S. and Erdogan, E. and Saracoglu, N.
dc.date.accessioned	2021-04-08T12:08:57Z
dc.date.available	2021-04-08T12:08:57Z
dc.date.issued	2015
dc.identifier	10.1002/jhet.2457
dc.identifier.issn	0022152X
dc.identifier.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84942552271&doi=10.1002%2fjhet.2457&partnerID=40&md5=03bedec8036bdcd4614fc3e36ecdcc60
dc.identifier.uri	http://acikerisim.bingol.edu.tr/handle/20.500.12898/4731
dc.description.abstract	Bi(NO3)3·5H2O-Catalyzed redox amination scope and mechanistic insights of benzylic ketones with indoline are discussed. The experimental results demonstrate that the formation of N-alkyl-substituted indole/indoline derivatives over typically competitive redox and reductive amination processes is depending upon the reaction condition for the benzylic ketones. © 2015 HeteroCorporation.
dc.language.iso	English
dc.source	Journal of Heterocyclic Chemistry
dc.title	Redox Amination Scope of Benzylic Ketones with Indoline: Synthetic and Mechanistic Insights

Files in this item

Files	Size	Format	View
There are no files associated with this item.

Scopus İndeksli Yayınlar Koleksiyonu [1357]
Scopus Indexed Publications Collection