Asymmetric Synthesis of Optically Active 1,1 prime -Bi-2-naphthol
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作者:
Su, Wu
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机构:
School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
Su, Wu
[1
]
Wang, Heng-Shan
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机构:
School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
Wang, Heng-Shan
[1
]
Da, Chao-Shan
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机构:
School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
Da, Chao-Shan
[1
]
Wang, Rui
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机构:
School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, ChinaSchool of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
Wang, Rui
[1
]
机构:
[1] School of Life Sciences, State Key Lab. of Appl. Organ. Chem., Lanzhou University, Lanzhou 730000, China
来源:
Kao Teng Hsueh Hsiao Hua Heush Hsueh Pao/ Chemical Journal of Chinese Universities
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2000年
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21卷
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09期
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摘要:
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).