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摘要:
Ketones smoothly reacted with NBS in the presence of a catalytic amount of ptoluenesulfonic acid to give α-bromoketones in good yields in typical ionic liquids, such as [bmim]PF6 and [bmpy]Tf2N, and the ionic liquids could be repeatedly used for the same reaction after the extraction of the α-bromoketones. Then, the one-pot conversion of ketones into thiazoles by the treatment with NBS, and subsequently with thioamides could be also carried out in [bmim]PF6 and [bmpy]Tf2N, respectively Thus, [bmim]PF6 and [bmpy]Tf2N could be used as recyclable reaction media for the preparation α-bromoketones and thiazoles from ketones.
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玉米自交系B73全基因组NBS类型抗病基因分析
玉米
生物信息学
抗病基因
核苷酸结合位点(NBS)
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篇名 Preparation of α-Bromoketones and Thiazoles from Ketones with NBS and Thioamides in Ionic Liquids
来源期刊 绿色与可持续化学(英文) 学科 化学
关键词 Ketone α-Bromoketone Thiazole NBS THIOAMIDE Ionic Liquid
年,卷(期) 2011,(3) 所属期刊栏目
研究方向 页码范围 54-62
页数 9页 分类号 O6
字数 语种
DOI
五维指标
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研究主题发展历程
节点文献
Ketone
α-Bromoketone
Thiazole
NBS
THIOAMIDE
Ionic
Liquid
研究起点
研究来源
研究分支
研究去脉
引文网络交叉学科
相关学者/机构
期刊影响力
绿色与可持续化学(英文)
季刊
2160-6951
武汉市江夏区汤逊湖北路38号光谷总部空间
出版文献量(篇)
188
总下载数(次)
0
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0
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