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 Publication | Tetrahedron:Asymmetry |
ISSN | 0957-4166 |
Volume | 20Pages:616-620 |
Abstract | Using 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 Organization | the National Natural Science Foundation of China (Nos. 20525206;20621091;20772052);the Chang Jiang Program of the Ministry of Education of China |
Indexed By | SCI |
Language | 英语 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://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 Author | Wang 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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