完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Kao, Tzu-Ting | en_US |
dc.contributor.author | Peng, Bo-Kai | en_US |
dc.contributor.author | Liang, Min-Chieh | en_US |
dc.contributor.author | Lee, Chia-Jui | en_US |
dc.contributor.author | Chen, I-Chia | en_US |
dc.contributor.author | Shia, Kak-Shan | en_US |
dc.contributor.author | Wu, Yen-Ku | en_US |
dc.date.accessioned | 2019-04-02T05:58:00Z | - |
dc.date.available | 2019-04-02T05:58:00Z | - |
dc.date.issued | 2018-12-07 | en_US |
dc.identifier.issn | 0022-3263 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/acs.joc.8b01866 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/148589 | - |
dc.description.abstract | Making use of temperature-controlled thiation as a key operation, a simple route to 2-aminothiophenes or thieno[2,3-c]isothiazoles has been newly developed wherein the 2-aminothiophene nucleus was formed through an initial formation of thioamide followed by a 5-exo-dig addition to the tethered alkyne; however, under harsher thermal conditions, excess sulfur-transferring reagents enabled further oxidative thiation to generate the corresponding thieno[2,3-c]isothiazoles. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Temperature-Controlled Thiation of alpha-Cyano-beta-Alkynyl Carbonyl Derivatives for De Novo Synthesis of 2-Aminothiophenes and Thieno[2,3-c]isothiazoles | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/acs.joc.8b01866 | en_US |
dc.identifier.journal | JOURNAL OF ORGANIC CHEMISTRY | en_US |
dc.citation.volume | 83 | en_US |
dc.citation.spage | 14688 | en_US |
dc.citation.epage | 14697 | 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:000452929900042 | en_US |
dc.citation.woscount | 0 | en_US |
顯示於類別: | 期刊論文 |