完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Lee, Yun-Ta | en_US |
dc.contributor.author | Chiu, Feng-Yu | en_US |
dc.contributor.author | Barve, Indrajeet J. | en_US |
dc.contributor.author | Sun, Chung-Ming | en_US |
dc.date.accessioned | 2018-08-21T05:53:16Z | - |
dc.date.available | 2018-08-21T05:53:16Z | - |
dc.date.issued | 2018-02-01 | en_US |
dc.identifier.issn | 1615-4150 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1002/adsc.201701140 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/144468 | - |
dc.description.abstract | An efficient and novel synthesis of benzimidazole-linked indoline hybrids via an unconventional Pictet-Spengler-type condensation of C-2 linked (o-aminobenzyl) benzimidazoles with aldehydes and ketones under microwave irradiation has been explored. The key condensation step consists of acid-catalyzed imine generation followed by intramolecular C-C bond formation through unique reactivity of the benzimidazole moiety. The scope of this method is further extended to synthesize tetracyclic pyrroloindole benzimidazole-carboxylates through 2-carboxaldehydes. | en_US |
dc.language.iso | en_US | en_US |
dc.subject | benzimidazole-linked indoles | en_US |
dc.subject | benzimidazole-linked indolines | en_US |
dc.subject | indoline synthesis | en_US |
dc.subject | pyrroloindolebenzimidazole-carboxylates | en_US |
dc.subject | unconventional Pictet-Spengler reaction | en_US |
dc.title | Microwave-Assisted Synthesis of Benzimidazole-Linked Indoline and Indole Hybrids from C-2 Linked (o-Aminobenzyl)benzimidazoles | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1002/adsc.201701140 | en_US |
dc.identifier.journal | ADVANCED SYNTHESIS & CATALYSIS | en_US |
dc.citation.volume | 360 | en_US |
dc.citation.spage | 502 | en_US |
dc.citation.epage | 512 | 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:000424093900019 | en_US |
顯示於類別: | 期刊論文 |