Please use this identifier to cite or link to this item:
https://scidar.kg.ac.rs/handle/123456789/12205
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.rights.license | restrictedAccess | - |
dc.contributor.author | Minić, Aleksandra | - |
dc.contributor.author | Stevanović, Dragana | - |
dc.contributor.author | Damljanović, Ivan | - |
dc.contributor.author | Pejović, Anka | - |
dc.contributor.author | Vukićević, Miomir | - |
dc.contributor.author | Bogdanovic, Goran A. | - |
dc.contributor.author | Radulovic, Niko | - |
dc.contributor.author | Vukicevic R. | - |
dc.date.accessioned | 2021-04-20T20:16:07Z | - |
dc.date.available | 2021-04-20T20:16:07Z | - |
dc.date.issued | 2015 | - |
dc.identifier.uri | https://scidar.kg.ac.rs/handle/123456789/12205 | - |
dc.description.abstract | © The Royal Society of Chemistry. A series of ferrocene-containing six-membered cyclic ureas (1-aryl-4-ferrocenyl-3-phenyltetrahydropyrimidin-2(1H)-ones) was synthesized (in high-to-excellent yields) by reacting the corresponding aminopropanols with phenyl isocyanate and the subsequent intramolecular cyclization of the thus obtained β-hydroxy ureas (prompted by acetic acid), via an α-ferrocenyl carbocation. This journal is | - |
dc.rights | info:eu-repo/semantics/restrictedAccess | - |
dc.source | RSC Advances | - |
dc.title | Synthesis of ferrocene-containing six-membered cyclic ureas via α-ferrocenyl carbocations | - |
dc.type | article | - |
dc.identifier.doi | 10.1039/c5ra01383f | - |
dc.identifier.scopus | 2-s2.0-84924871534 | - |
Appears in Collections: | Faculty of Science, Kragujevac |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
PaperMissing.pdf Restricted Access | 29.86 kB | Adobe PDF | ![]() View/Open |
Items in SCIDAR are protected by copyright, with all rights reserved, unless otherwise indicated.