Convenient preparation of chiral alpha,beta-epoxy ketones via Claisen-Schmidt condensation-epoxidation sequence
文献类型:期刊论文
作者 | Wang, Yongcan; Ye, Jinxing; Liang, Xinmiao |
刊名 | advanced synthesis & catalysis
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出版日期 | 2007-05-01 |
卷号 | 349期号:7页码:1033-1036 |
关键词 | aldehydes asymmetric catalysis condensation epoxidation ketones one-pot |
英文摘要 | a novel clasisen-schmidt condensation-epoxidation sequence of aldehydes and ketones was developed to produce a series of chiral ap-epoxy ketones under asymmetric phase-transfer catalytic conditions. the organocatalytic method reported here can afford chiral alpha,beta-epoxy ketones under mild conditions with moderate to good yields and up to 96% ee. |
WOS标题词 | science & technology ; physical sciences |
类目[WOS] | chemistry, applied ; chemistry, organic |
研究领域[WOS] | chemistry |
关键词[WOS] | catalytic asymmetric epoxidation ; highly enantioselective epoxidation ; transfer mediated epoxidation ; phase-transfer catalysts ; alpha,beta-unsaturated ketones ; trichloroisocyanuric acid ; cinchona alkaloids ; enones ; water |
收录类别 | SCI ; CCR |
语种 | 英语 |
WOS记录号 | WOS:000246990200006 |
公开日期 | 2015-11-17 |
源URL | [http://159.226.238.44/handle/321008/140394] ![]() |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
作者单位 | 1.E China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China 2.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China |
推荐引用方式 GB/T 7714 | Wang, Yongcan,Ye, Jinxing,Liang, Xinmiao. Convenient preparation of chiral alpha,beta-epoxy ketones via Claisen-Schmidt condensation-epoxidation sequence[J]. advanced synthesis & catalysis,2007,349(7):1033-1036. |
APA | Wang, Yongcan,Ye, Jinxing,&Liang, Xinmiao.(2007).Convenient preparation of chiral alpha,beta-epoxy ketones via Claisen-Schmidt condensation-epoxidation sequence.advanced synthesis & catalysis,349(7),1033-1036. |
MLA | Wang, Yongcan,et al."Convenient preparation of chiral alpha,beta-epoxy ketones via Claisen-Schmidt condensation-epoxidation sequence".advanced synthesis & catalysis 349.7(2007):1033-1036. |
入库方式: OAI收割
来源:大连化学物理研究所
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