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典型文献
Highly enantioselective construction of CF3-bearing all-carbon quaternary stereocenters:Chiral spiro-fused bisoxazoline ligands with 1,1'-binaphthyl sidearm for asymmetric Michael-type Friedel-Crafts reaction
文献摘要:
A novel class of chiral spiro-fused bisoxazoline ligands possessing a deep chiral pocket was prepared.The developed ligands have been employed in the nickel-catalyzed highly enantioselective Michael-type Friedel-Crafts reaction,affording the products bearing a trifluoromethylated all-carbon quaternary stere-ocenter with moderate to excellent yields(up to 99%)and good to excellent enantioselectivies(up to>99.9%ee).Moreover,a proposed model of chiral pocket revealed that the attack of indole from the Re-face of β-CF3-β-disubstituted nitroalkene was favorable.
文献关键词:
作者姓名:
Robert Li-Yuan Bao;Lei Shi;Kang Fu
作者机构:
School of Science,Harbin Institute of Technology,Shenzhen 518055,China;State Key Laboratory of Elemento-Organic Chemistry,Nankai University,Tianjin 300071,China;Guangdong Provincial Key Laboratory of Catalysis,Southern University of Science and Technology,Shenzhen 518055,China;School of Chemistry and Chemical Engineering,Harbin Institute of Technology,Harbin 150001,China
引用格式:
[1]Robert Li-Yuan Bao;Lei Shi;Kang Fu-.Highly enantioselective construction of CF3-bearing all-carbon quaternary stereocenters:Chiral spiro-fused bisoxazoline ligands with 1,1'-binaphthyl sidearm for asymmetric Michael-type Friedel-Crafts reaction)[J].中国化学快报(英文版),2022(05):2415-2419
A类:
stereocenters,bisoxazoline,sidearm,trifluoromethylated,stere,ocenter,enantioselectivies,nitroalkene
B类:
Highly,enantioselective,construction,CF3,bearing,all,carbon,quaternary,Chiral,spiro,fused,ligands,binaphthyl,asymmetric,Michael,type,Friedel,Crafts,reaction,novel,class,chiral,possessing,deep,pocket,was,prepared,developed,have,been,employed,nickel,catalyzed,highly,affording,products,moderate,excellent,yields,up,good,Moreover,proposed,model,revealed,that,attack,indole,from,Re,face,disubstituted,favorable
AB值:
0.518668
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