Synthesis of highly N-substituted indole library via conjugate additions of indoline and their synthetic tool potentials

dc.contributor.author	Kilic, H. and Bayindir, S. and Erdogan, E. and Saracoglu, N.
dc.date.accessioned	2021-04-08T12:10:04Z
dc.date.available	2021-04-08T12:10:04Z
dc.date.issued	2012
dc.identifier	10.1016/j.tet.2012.04.066
dc.identifier.issn	00404020
dc.identifier.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84862021404&doi=10.1016%2fj.tet.2012.04.066&partnerID=40&md5=0de4a98fd858a24a88a634cdaf5a16ec
dc.identifier.uri	http://acikerisim.bingol.edu.tr/handle/20.500.12898/4953
dc.description.abstract	A comprehensive library of N- or 1-substituted indoles was formed by conjugate additions of indoline with Michael acceptors followed by an oxidation step. Using N-substituted indoles as key Michael donors, the synthesis of 1,3-disubstituted indoles was also accomplished. © 2012 Elsevier Ltd. All rights reserved.
dc.language.iso	English
dc.source	Tetrahedron
dc.title	Synthesis of highly N-substituted indole library via conjugate additions of indoline and their synthetic tool potentials

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