中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
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
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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