Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication
| dc.citation.epage | 97120 | en_US |
| dc.citation.issue | 118 | en_US |
| dc.citation.spage | 97113 | en_US |
| dc.citation.volume | 5 | en_US |
| dc.citation.woscount | 1 | en_US |
| dc.contributor.author | Chang, Wong-Jin | en_US |
| dc.contributor.author | Kulkarni, Manohar V. | en_US |
| dc.contributor.author | Sun, Chung-Ming | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2019-04-03T06:36:37Z | |
| dc.date.available | 2019-04-03T06:36:37Z | |
| dc.date.issued | 2015-01-01 | en_US |
| dc.description.abstract | A one-pot multi component reaction of selenoureas, which are in situ generated from L-amino esters and isoselenocyanates, with alpha-bromoketone under ultrasonication. Selenourea and alpha-bromoketones formed 2-iminoselenazoles through a Hantzsch selenazole-type reaction. The steric effect of the alpha-substituted bromoketones on the rate of the tandem reaction was studied to understand the reaction mechanism by isolating the key reaction intermediate, 2-iminoselenol. | en_US |
| dc.identifier.doi | 10.1039/c5ra18763j | en_US |
| dc.identifier.issn | 2046-2069 | en_US |
| dc.identifier.journal | RSC ADVANCES | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1039/c5ra18763j | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/129446 | |
| dc.identifier.wosnumber | WOS:000365220100004 | en_US |
| dc.language.iso | en_US | en_US |
| dc.title | Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication | en_US |
| dc.type | Article | en_US |