Condensation of Indoline with Some 1,2- and 1,3-Diketones

dc.contributor.author	Kilic, H. and Aydin, O. and Bayindir, S. and Saracoglu, N.
dc.date.accessioned	2021-04-08T12:08:28Z
dc.date.available	2021-04-08T12:08:28Z
dc.date.issued	2016
dc.identifier	10.1002/jhet.2580
dc.identifier.issn	0022152X
dc.identifier.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84952690371&doi=10.1002%2fjhet.2580&partnerID=40&md5=484e880306a23151ff3e17081a195348
dc.identifier.uri	http://acikerisim.bingol.edu.tr/handle/20.500.12898/4607
dc.description.abstract	Bismuth nitrate catalyzed condensation reactions of indoline with 1,2- and 1,3-diketones were investigated and were reported to proceed via different reaction pathways with the involvement of one or two of the carbonyl groups. While the reaction of indoline with cyclohexane-1,3-dione (4) gave solely condensation product, the reaction between the acetylacetone (5) and indoline provided N-acetyl indoline as single products on retro-aldol process. In contrast to 1,3-diketones, the reaction with benzil (17) was performed under difficult conditions and proceeded to give secondary products. © 2015 HeteroCorporation
dc.language.iso	English
dc.source	Journal of Heterocyclic Chemistry
dc.title	Condensation of Indoline with Some 1,2- and 1,3-Diketones

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