Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-Disubstituted Quinolines
Wang, Da-Wei1; Wang, Xiao-Bing1; Wang, Duo-Sheng1; Lu, Sheng-Mei1; Zhou, Yong-Gui1,2; Li, Yu-Xue2
刊名journal of organic chemistry
2009-04-03
卷号74期号:7页码:2780-2787
英文摘要the enantioselective hydrogenation of 2-benzylquinolines and 2-functionalized and 2,3-disubstituted quinolines was developed by using the [ir(cod)cl]2/bisphosphine/i(2) system with up to 96% ee. moreover, mechanistic studies revealed the hydrogenation mechanism of quinoline involves a 1,4-hydride addition, isomerization, and 1,2-hydride addition, and the catalytic active species may be a ir(iii) complex with chloride and iodide.
WOS标题词science & technology ; physical sciences
类目[WOS]chemistry, organic
研究领域[WOS]chemistry
关键词[WOS]asymmetric transfer hydrogenation ; n-iminopyridinium ylides ; ir-f-binaphane ; heteroaromatic-compounds ; homogeneous hydrogenation ; hantzsch esters ; complexes ; ligands ; derivatives ; indoles
收录类别SCI ; IC ; CCR
语种英语
WOS记录号WOS:000264627400018
公开日期2015-11-17
内容类型期刊论文
源URL[http://159.226.238.44/handle/321008/141246]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
2.Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
推荐引用方式
GB/T 7714
Wang, Da-Wei,Wang, Xiao-Bing,Wang, Duo-Sheng,et al. Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-Disubstituted Quinolines[J]. journal of organic chemistry,2009,74(7):2780-2787.
APA Wang, Da-Wei,Wang, Xiao-Bing,Wang, Duo-Sheng,Lu, Sheng-Mei,Zhou, Yong-Gui,&Li, Yu-Xue.(2009).Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-Disubstituted Quinolines.journal of organic chemistry,74(7),2780-2787.
MLA Wang, Da-Wei,et al."Highly Enantioselective Iridium-Catalyzed Hydrogenation of 2-Benzylquinolines and 2-Functionalized and 2,3-Disubstituted Quinolines".journal of organic chemistry 74.7(2009):2780-2787.
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