中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
L-prolinamide-catalyzed direct nitroso aldol reactions of alpha-branched aldehydes: a distinct regioselectivity from that with l-proline

文献类型:期刊论文

作者Guo, HM; Cheng, L; Cun, LF; Gong, LZ; Mi, AQ; Jiang, YZ
刊名Chemical communications
出版日期2006-01-28
期号4页码:429-431
ISSN号1359-7345
DOI10.1039/b514194j
通讯作者Gong, lz()
英文摘要The first direct enantioselective n-nitroso aldol reaction of aldehyde with nitrosobenzene catalyzed by an l-prolinamide derivative is presented; the reactions proceed smoothly furnishing the a-hydroxyamino carbonyl compounds, the otherwise disfavored products, in good yields with up to 64% ee.
WOS关键词CARBONYL-COMPOUNDS ; AMINOXYLATION ; KETONES ; AMINOOXYLATION ; OXIDATION ; 1,2-DIOLS ; ALCOHOLS ; ENAMINE ; HYDROXY ; ROUTE
WOS研究方向Chemistry
WOS类目Chemistry, Multidisciplinary
语种英语
WOS记录号WOS:000235034800020
出版者ROYAL SOC CHEMISTRY
URI标识http://www.irgrid.ac.cn/handle/1471x/2379235
专题中国科学院大学
通讯作者Gong, LZ
作者单位1.Chinese Acad Sci, Key Lab Asymmetr Synth & Chirotechnol Sichuan Pro, Chengdu 610041, Peoples R China
2.Chinese Acad Sci, Union Lab Asymmetr Synth, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
3.Henan Normal Univ, Dept Chem, Xinxiang 453002, Henan, Peoples R China
4.Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
推荐引用方式
GB/T 7714
Guo, HM,Cheng, L,Cun, LF,et al. L-prolinamide-catalyzed direct nitroso aldol reactions of alpha-branched aldehydes: a distinct regioselectivity from that with l-proline[J]. Chemical communications,2006(4):429-431.
APA Guo, HM,Cheng, L,Cun, LF,Gong, LZ,Mi, AQ,&Jiang, YZ.(2006).L-prolinamide-catalyzed direct nitroso aldol reactions of alpha-branched aldehydes: a distinct regioselectivity from that with l-proline.Chemical communications(4),429-431.
MLA Guo, HM,et al."L-prolinamide-catalyzed direct nitroso aldol reactions of alpha-branched aldehydes: a distinct regioselectivity from that with l-proline".Chemical communications .4(2006):429-431.

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来源:中国科学院大学

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