LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions
Department羰基合成与选择氧化国家重点实验室
Zhou W(周伟); Xu LW(徐利文); Qiu HY(邱化玉); Lai GQ(来国桥); Xia CG(夏春谷); Jiang JX(蒋剑雄)
2008
Source PublicationHelvetica Chimica Acta
ISSN0018-019X
Volume91Pages:53-59
AbstractA novel chiral ionic liquid, compound 1, based on camphorsulfonic acid, was prepared. A catalytic amount of 1 readily promotes l-proline-catalyzed aldol reactions, with good chemoselectivity, both in H2O and in organic solvents. Further, the aldol reaction of cyclohexanone with 4-nitrobenzaldehyde afforded 2-[hydroxy(4-nitrophenyl)methyl]cyclohexanone (6) in 98% yield with high enantioselectivity (94% ee) when large amounts of 1 (5 equiv.) were used as promoter.
Subject Area清洁催化与生物转化
Funding Organizationthe National Natural Science Foundation of China (20572114)
Indexed BySCI
Language英语
Funding Project清洁催化与生物转化研究组
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/1973
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorXu LW(徐利文); Lai GQ(来国桥); Xia CG(夏春谷)
Recommended Citation
GB/T 7714
Zhou W,Xu LW,Qiu HY,et al. Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions[J]. Helvetica Chimica Acta,2008,91:53-59.
APA 周伟,徐利文,邱化玉,来国桥,夏春谷,&蒋剑雄.(2008).Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions.Helvetica Chimica Acta,91,53-59.
MLA 周伟,et al."Synthesis of a novel chiral ionic liquid and its application in enantioselective aldol reactions".Helvetica Chimica Acta 91(2008):53-59.
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