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Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine; Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine
Hu, XP; Chen, HL; Dai, HC; Zheng, Z
刊名TETRAHEDRON-ASYMMETRY ; TETRAHEDRON-ASYMMETRY
2003-10-31 ; 2003-10-31
DOI10.1016/j.tetasy.2003.09.034 ; 10.1016/j.tetasy.2003.09.034
14期:21页:3415-3421
收录类别SCI ; SCI ; IC ; IC ; CCR ; CCR
文章类型Article ; Article
部门归属206 ; 206
项目归属206 ; 206
产权排名1;1 ; 1;1
WOS标题词Science & Technology ; Science & Technology ; Physical Sciences ; Physical Sciences
类目[WOS]Chemistry, Inorganic & Nuclear ; Chemistry, Inorganic & Nuclear ; Chemistry, Organic ; Chemistry, Organic ; Chemistry, Physical ; Chemistry, Physical
研究领域[WOS]Chemistry ; Chemistry
关键词[WOS]ASYMMETRIC ALLYLIC ALKYLATION ; ASYMMETRIC ALLYLIC ALKYLATION ; TRANSITION-METAL-COMPLEXES ; TRANSITION-METAL-COMPLEXES ; ENANTIOSELECTIVE HYDROSILYLATION ; ENANTIOSELECTIVE HYDROSILYLATION ; SUBSTITUTION-REACTIONS ; SUBSTITUTION-REACTIONS ; AMIDINE LIGANDS ; AMIDINE LIGANDS ; HYBRID LIGANDS ; HYBRID LIGANDS ; IMINE LIGANDS ; IMINE LIGANDS ; PALLADIUM ; PALLADIUM ; KETONES ; KETONES ; BACKBONE ; BACKBONE
英文摘要A series of novel ferrocenylphosphine-ketimine ligands 6 were prepared by reaction of (R,S-p)-PPFNH2-R or (S,S-p)-PPFNH2 with a variety of m-substituted acetophenones. A different catalytic activity was observed between ferrocenylphosphine-ketimine ligands and corresponding aldimine ligands. The efficiency and diastereomeric impact of these ferrocenylphosphine-ketimine ligands in Pd-catalyzed asymmetric allylic alkylation were first investigated, and higher enantioselectivity of over 98% e.e. with 95% yield was obtained by the use of ferrocenylphosphine-ketimine ligands. However, in Rh-catalyzed asymmetric hydrosilylation of aryl ketones, only 42% e.e. was obtained by the use of ferrocenylphosphine-ketimine ligands compared to 90% e.e. with the use of aldimine ligands. (C) 2003 Elsevier Ltd. All rights reserved.; A series of novel ferrocenylphosphine-ketimine ligands 6 were prepared by reaction of (R,S-p)-PPFNH2-R or (S,S-p)-PPFNH2 with a variety of m-substituted acetophenones. A different catalytic activity was observed between ferrocenylphosphine-ketimine ligands and corresponding aldimine ligands. The efficiency and diastereomeric impact of these ferrocenylphosphine-ketimine ligands in Pd-catalyzed asymmetric allylic alkylation were first investigated, and higher enantioselectivity of over 98% e.e. with 95% yield was obtained by the use of ferrocenylphosphine-ketimine ligands. However, in Rh-catalyzed asymmetric hydrosilylation of aryl ketones, only 42% e.e. was obtained by the use of ferrocenylphosphine-ketimine ligands compared to 90% e.e. with the use of aldimine ligands. (C) 2003 Elsevier Ltd. All rights reserved.
语种英语 ; 英语
原文出处查看原文 ; 查看原文
WOS记录号WOS:000186352300024 ; WOS:000186352300024
引用统计
被引频次:20[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://cas-ir.dicp.ac.cn/handle/321008/82831
专题中国科学院大连化学物理研究所
作者单位Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
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GB/T 7714
Hu, XP,Chen, HL,Dai, HC,et al. Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine, Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine[J]. TETRAHEDRON-ASYMMETRY, TETRAHEDRON-ASYMMETRY,2003, 2003,14, 14(21):3415-3421, 3415-3421.
APA Hu, XP,Chen, HL,Dai, HC,&Zheng, Z.(2003).Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine.TETRAHEDRON-ASYMMETRY,14(21),3415-3421.
MLA Hu, XP,et al."Synthesis of novel P-ketimine bidentate ferrocenyl ligands with central and planar chirality and comparsion in the catalytic activity between P-ketimine and P-aldimine".TETRAHEDRON-ASYMMETRY 14.21(2003):3415-3421.
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