完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.author | Fukuyama, Takahide | en_US |
| dc.contributor.author | Okada, Takuma | en_US |
| dc.contributor.author | Nakashima, Nao | en_US |
| dc.contributor.author | Ryu, Ilhyong | en_US |
| dc.date.accessioned | 2019-12-13T01:12:16Z | - |
| dc.date.available | 2019-12-13T01:12:16Z | - |
| dc.date.issued | 2019-10-01 | en_US |
| dc.identifier.issn | 0018-019X | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1002/hlca.201900186 | en_US |
| dc.identifier.uri | http://hdl.handle.net/11536/153144 | - |
| dc.description.abstract | Formal [2+2+1] cycloaddition reaction involving acetylenes, aromatic imines, and CO was achieved by radical chain reaction, which gave five-membered unsaturated lactams in modest to good yields. When we used 5-chloropentyne, sequential carbonylation took place accompanied with double annulation events to give a cyclohexanone-fused lactam in excellent stereoselectivity. | en_US |
| dc.language.iso | en_US | en_US |
| dc.subject | cycloaddition | en_US |
| dc.subject | alkynes | en_US |
| dc.subject | CO | en_US |
| dc.subject | aromatic imines | en_US |
| dc.subject | lactams | en_US |
| dc.title | Radical Mediated Aza-Pauson-Khand Reaction of Acetylenes, Imines, and CO Leading to Five-Membered Unsaturated Lactams | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.1002/hlca.201900186 | en_US |
| dc.identifier.journal | HELVETICA CHIMICA ACTA | en_US |
| dc.citation.volume | 102 | en_US |
| dc.citation.issue | 10 | en_US |
| dc.citation.spage | 0 | en_US |
| dc.citation.epage | 0 | 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:000496451400002 | en_US |
| dc.citation.woscount | 0 | en_US |
| 顯示於類別: | 期刊論文 | |

