中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to alpha,beta,gamma,delta-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups

文献类型:期刊论文

作者Lu JZ(陆俊筑)1; Ye JX(叶金星)1; Duan WL(段伟良)1
刊名Chem. Commun.
出版日期2014
卷号50期号:6页码:698-700
其他题名钯催化二芳基膦氢对α,β,γ,δ-磺酸酯不饱和共轭二烯的不对称1,6加成反应
通讯作者段伟良
英文摘要Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to electron-deficient dienes was developed through rational selection of electron-withdrawing groups on the dienes. Various chiral allylic phosphine derivatives were synthesized in good yields with high enantioselectivity (up to 96% ee).
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1039/c3cc46290k
语种英语
源URL[http://ir.sioc.ac.cn/handle/331003/39024]  
专题上海有机化学研究所_金属有机化学国家重点实验室
作者单位1.中科院上海有机化学研究所
2.华东理工大学
推荐引用方式
GB/T 7714
Lu JZ,Ye JX,Duan WL. Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to alpha,beta,gamma,delta-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups[J]. Chem. Commun.,2014,50(6):698-700.
APA 陆俊筑,叶金星,&段伟良.(2014).Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to alpha,beta,gamma,delta-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups.Chem. Commun.,50(6),698-700.
MLA 陆俊筑,et al."Palladium-catalyzed asymmetric 1,6-addition of diarylphosphines to alpha,beta,gamma,delta-unsaturated sulfonic esters: controlling regioselectivity by rational selection of electron-withdrawing groups".Chem. Commun. 50.6(2014):698-700.

入库方式: OAI收割

来源:上海有机化学研究所

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