完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Selvaraju, Manikandan | en_US |
dc.contributor.author | Shiu, Wei-Shuen | en_US |
dc.contributor.author | Kulkarni, Manohar V. | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2014-12-08T15:32:46Z | - |
dc.date.available | 2014-12-08T15:32:46Z | - |
dc.date.issued | 2013 | en_US |
dc.identifier.issn | 2046-2069 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/22901 | - |
dc.identifier.uri | http://dx.doi.org/10.1039/c3ra42658k | en_US |
dc.description.abstract | A telescoped sequence involves the reaction of cationic imidazolium attached 2-aminobenzimidazoles with in situ generated 1,1-dicyano-2-aryl ethylenes was explored for the regioselective synthesis of pyrimido[1,2-a]benzimidazoles. The perceived regioselectivity was presumed in terms of preferential Michael addition of 2-aminobenzimidazole followed by intramolecular annulation to the exclusive formation of 4-iminopyrimidines on an ionic liquid support. A plausible mechanistic pathway for their selective formation is discussed and fully supported by X-ray analysis. The present strategy reveals both the amine function and the ring nitrogen in substituted 2-aminobenzimidazoles are active sites for nucleophilic attack on alpha,beta-unsaturated nitriles. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Ionic liquid supported synthesis of tricyclic pyrimido [1,2-a]benzimidazoles by a telescoped Michael/hetero annulation strategy | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1039/c3ra42658k | en_US |
dc.identifier.journal | RSC ADVANCES | en_US |
dc.citation.volume | 3 | en_US |
dc.citation.issue | 44 | en_US |
dc.citation.spage | 22314 | en_US |
dc.citation.epage | 22318 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000326056600164 | - |
dc.citation.woscount | 0 | - |
顯示於類別: | 期刊論文 |