Asymmetric Synthesis of Optically Active 1,1 prime -Bi-2-naphthol

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作者
Su, Wu [1 ]
Wang, Heng-Shan [1 ]
Da, Chao-Shan [1 ]
Wang, Rui [1 ]
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[1] School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
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Experimental results are reported for the CuCl2-mediated asymmetric oxidative coupling of 2-naphthols in the presence of [-]α-methylbenzylamine to optically active (S)-(-)-1,1 prime -bi-2-naphthol. Under anhydrous conditions and with a 3:1 molarity ratio of α-methylbenzylamine to 2-naphthol, a fair enantioselection has been observed (up to 80. 6% ee).
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