完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Dhole, Sandip | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2019-04-02T06:00:30Z | - |
dc.date.available | 2019-04-02T06:00:30Z | - |
dc.date.issued | 2019-02-01 | en_US |
dc.identifier.issn | 1615-4150 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1002/adsc.201801241 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/148827 | - |
dc.description.abstract | A facile and straightforward synthesis of benzoimidazo[2,1-a]isoquinolines through Ru(II)-catalyzed [4+2] annulation reaction of 2-aryl benzimidazole and styrene has been explored. Tentative mechanistic studies imply the current reaction involves sequential C-C/C-N bond formation through the ortho C-H activation of 2-aryl benzimidazole followed by C-N reductive elimination. This newly developed strategy is widely applicable and tolerates various 2-arylbenzimidazole and vinyl derivatives, and allows the attractive vehicle for direct construction of diverse C6-substituated benzoimidazoisoquinoline scaffold in good yields. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | Benzoimidazo[2,1-a]isoquinolines Ruthenium | en_US |
dc.subject | [4+2] annulation | en_US |
dc.subject | 2-aryl benzimidazole | en_US |
dc.subject | Styrene | en_US |
dc.title | Direct Access to Dihydrobenzoimidazo[2,1-a]isoquinolines through Ruthenium-catalyzed Formal [4+2] Annulation | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/adsc.201801241 | en_US |
dc.identifier.journal | ADVANCED SYNTHESIS & CATALYSIS | en_US |
dc.citation.volume | 361 | en_US |
dc.citation.spage | 535 | en_US |
dc.citation.epage | 541 | 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:000457795500021 | en_US |
dc.citation.woscount | 0 | en_US |
顯示於類別: | 期刊論文 |