Application of ferrocenyl substituted aziridinylmethanols (FAM) as chiral ligands in enantioselective conjugate addition of diethylzinc to enones
摘要:
Easily available ferrocenyl substituted aziridinylmethanol FAM-4a complexes with nickel and catalyzes the enantioselective diethylzinc addition to various enones with enantiomeric excesses reaching 80%. The ligand can be recovered and used without losing its activity. The sense of induction was found to be dependent on the configuration of the aziridine ring. (c) 2007 Elsevier Ltd. All rights reserved.
The copper-catalyzed enantioselectiveconjugateaddition of diethylzinc to acyclic enones was achieved with chiral sulfoxide–phosphine (SOP) ligands. This process showed good functional group tolerance and gave the 1, 4-adducts with excellent enantioselectivities (up to 96% ee).
Highly enantioselective conjugate addition of diethylzinc to substituted chalcones catalyzed by Cu(II) complexes of a tridentate P,N,O ligand
作者:Deepak Baburao Biradar、Han-Mou Gau
DOI:10.1016/j.tetasy.2008.02.027
日期:2008.4
A new series of tridentate P,N,O ligands having hard and soft donor atoms derived from chiral amino alcohols were developed and employed in the Cu(II)-catalyzed conjugate addition of diethylzinc to substituted chalcones. The asymmetric additions to a variety of substituted chalcones afforded products in excellent yields and good to excellent enantioselectivities up to 97% ee. (c) 2008 Elsevier Ltd. All rights reserved.
Enantioselective copper(II)-catalyzed conjugate addition of diethylzinc to β-substituted enones utilizing BINOL-based phosphoramidite ligands
作者:Wenxian Zhao、Tao Wang、Ruijuan Zhao、Huanping Xie、Lantao Liu
DOI:10.1016/j.tetasy.2016.01.016
日期:2016.3
A family of new chiral phosphoramidite ligands based on 3,3'-disubstituted (S)-BINOL have been successfully synthesized. The chiral phosphoramidite ligands were subsequently applied to the copper(II)-catalyzed enantioselective addition of diethylzinc to beta-substituted enones, giving the desired chiral adducts with enantioselectivities of up to 93% ee and high yields (up to 88%). (C) 2016 Elsevier Ltd. All rights reserved.
Enantioselective conjugate addition of dialkylzincs to α,β-unsaturated enones catalyzed by Ni(acac)2 and (+)-(1S,2R)-7,7-dimethyl-1-morpholinoisonorborneol
作者:Chih-Hao Tseng、Yu-Ming Hung、Biing-Jiun Uang
DOI:10.1016/j.tetasy.2012.01.010
日期:2012.1
A mixture of chiral ligand 4 [(+)-MINBOL] and Ni(acac)(2) (12.5 and 0.5 mol % respectively) is able to successfully catalyze the enantioselective conjugate 1,4-addition of dialkylzinc to alpha,beta-unsaturated enones in propionitrile to give the corresponding chiral Michael adducts in good yields and with high enantioselectivities (up to 93% ee). (C) 2012 Elsevier Ltd. All rights reserved.
Enantioselective conjugate addition of diethylzinc to chalcones catalysed by N-trityl aziridine-2-(S)-(diphenyl)methanol and Ni(acac)2
作者:Uma Shadakshari、Sandip K Nayak
DOI:10.1016/s0040-4020(01)00793-1
日期:2001.9
The chiral Ni(II) complex prepared from Ni(acac)(2) and N-trityl aziridine-2-(S)-(diphenyl)methanol catalyses the enantioselective conjugate addition of diethylzinc to chalcones in good yield with ces of upto 93%. (C) 2001 Elsevier Science Ltd. All rights reserved.