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 | |