中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Asymmetric Transfer Hydrogenations of 2,3-Disubstituted Quinoxalines with Ammonia Borane

文献类型:期刊论文

作者Li, Songlei1,2; Meng, Wei1,2; Du, Haifeng1,2
刊名ORGANIC LETTERS
出版日期2017-05-19
卷号19期号:10页码:2604-2606
英文摘要An asymmetric transfer hydrogenation of 2,3-disubstituted quinoxalines using a chiral frustrated Lewis pair of Piers' borane and (R)-tert-butylsulfinamide as the catalyst with ammonia borane as the hydrogen source has been successfully realized. For 2-alkyl-3-arylquinoxaline substrates cis-tetrahydroquinoxalines were obtained as the predominant products in high yields with 77-86% ee. In contrast trans isomers were often furnished as major products for the reactions of 2,3-dialkylquinoxalines with up to >99% ee.
语种英语
源URL[http://ir.iccas.ac.cn/handle/121111/38398]  
专题化学研究所_分子识别与功能实验室
作者单位1.Chinese Acad Sci, Inst Chem, CAS Res Educ Ctr Excellence Mol Sci, Beijing Natl Lab Mol Sci,CAS Key Lab Mol Recognit, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
推荐引用方式
GB/T 7714
Li, Songlei,Meng, Wei,Du, Haifeng. Asymmetric Transfer Hydrogenations of 2,3-Disubstituted Quinoxalines with Ammonia Borane[J]. ORGANIC LETTERS,2017,19(10):2604-2606.
APA Li, Songlei,Meng, Wei,&Du, Haifeng.(2017).Asymmetric Transfer Hydrogenations of 2,3-Disubstituted Quinoxalines with Ammonia Borane.ORGANIC LETTERS,19(10),2604-2606.
MLA Li, Songlei,et al."Asymmetric Transfer Hydrogenations of 2,3-Disubstituted Quinoxalines with Ammonia Borane".ORGANIC LETTERS 19.10(2017):2604-2606.

入库方式: OAI收割

来源:化学研究所

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