Acid controlled diastereoselectivity in asymmetric aldol reaction of cycloketones with aldehydes using enamine-based organocatalysts
文献类型:期刊论文
作者 | Gao, Jinsuo1,2; Bai, Shiyang1; Gao, Qiang1; Liu, Yan1; Yang, Qihua1 |
刊名 | chemical communications
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出版日期 | 2011 |
卷号 | 47期号:23页码:6716-6718 |
ISSN号 | 待补充 |
产权排序 | 1,1 |
通讯作者 | 杨启华 ; 刘 |
中文摘要 | acid controlled diastereoselectivity in asymmetric aldol reaction of cycloketones with aldehydes using enamine-based organocatalysts |
英文摘要 | the example of syn-aldol reaction of cyclohexanone to aldehyde was demonstrated based on chiral diamine organocatalysts and it was realized either by increasing the molecular size of acid additives or by introducing a hydrogen-bond donor into acid additives. |
WOS标题词 | science & technology ; physical sciences |
学科主题 | 物理化学 |
类目[WOS] | chemistry, multidisciplinary |
研究领域[WOS] | chemistry |
关键词[WOS] | mannich-type reactions ; diels-alder reactions ; aliphatic-ketones ; anti-mannich ; catalysis ; water ; dihydroxyacetone ; stereocenters ; proline ; michael |
收录类别 | SCI ; CCR |
语种 | 英语 |
WOS记录号 | WOS:000291113000061 |
公开日期 | 2012-07-09 |
源URL | [http://159.226.238.44/handle/321008/115275] ![]() |
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.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China 2.Dalian Univ Technol, Key Lab Ind Ecol & Environm Engn, Minist Educ, Sch Environm Sci & Technol, Dalian 116024, Peoples R China |
推荐引用方式 GB/T 7714 | Gao, Jinsuo,Bai, Shiyang,Gao, Qiang,et al. Acid controlled diastereoselectivity in asymmetric aldol reaction of cycloketones with aldehydes using enamine-based organocatalysts[J]. chemical communications,2011,47(23):6716-6718. |
APA | Gao, Jinsuo,Bai, Shiyang,Gao, Qiang,Liu, Yan,&Yang, Qihua.(2011).Acid controlled diastereoselectivity in asymmetric aldol reaction of cycloketones with aldehydes using enamine-based organocatalysts.chemical communications,47(23),6716-6718. |
MLA | Gao, Jinsuo,et al."Acid controlled diastereoselectivity in asymmetric aldol reaction of cycloketones with aldehydes using enamine-based organocatalysts".chemical communications 47.23(2011):6716-6718. |
入库方式: OAI收割
来源:大连化学物理研究所
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