LICP OpenIR  > 羰基合成与选择氧化国家重点实验室(OSSO)
Enantioselective addition of thiophenylboronic acids to aldehydes using ZnEt2/Schiff-base catalytic system
Department羰基合成与选择氧化国家重点实验室
Liu XD(刘晓东); Qiu L(邱立); Hong L(洪亮); Yan WJ(阎文锦); Wang R(王锐)
2009
Source PublicationTetrahedron:Asymmetry
ISSN0957-4166
Volume20Pages:616-620
AbstractUsing Schiff-base amino alcohols as catalysts which were readily derived from natural amino acids in three steps, a series of valuable optically active thiophenyl methanols (4a–4n) were first obtained in good yields and high enantioselectivities (up to 96% ee) through the asymmetric addition of thiophenylboronic acid to aldehydes in the presence of ZnEt2 in toluene.
Subject Area物理化学
Funding Organizationthe National Natural Science Foundation of China (Nos. 20525206;20621091;20772052);the Chang Jiang Program of the Ministry of Education of China
Indexed BySCI
Language英语
Citation statistics
Cited Times:13[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/579
Collection羰基合成与选择氧化国家重点实验室(OSSO)
Corresponding AuthorWang R(王锐)
Recommended Citation
GB/T 7714
Liu XD,Qiu L,Hong L,et al. Enantioselective addition of thiophenylboronic acids to aldehydes using ZnEt2/Schiff-base catalytic system[J]. Tetrahedron:Asymmetry,2009,20:616-620.
APA 刘晓东,邱立,洪亮,阎文锦,&王锐.(2009).Enantioselective addition of thiophenylboronic acids to aldehydes using ZnEt2/Schiff-base catalytic system.Tetrahedron:Asymmetry,20,616-620.
MLA 刘晓东,et al."Enantioselective addition of thiophenylboronic acids to aldehydes using ZnEt2/Schiff-base catalytic system".Tetrahedron:Asymmetry 20(2009):616-620.
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