Bulletin of the Chemical Society of Japan p. 956 - 957 (1989)
Update date:2022-08-30
Topics:
Oi, Shuichi
Matsuzaka, Yutaka
Yamashita, Junzo
Miyano, Sotaro
Both enentiomers of 1,1'-binaphthyl-2,2'-dicarboxylic acid (100percent ee's by HPLC) were conveniently obtained in high yields (ca. 80percent of the theory) via fractional crystallization of the (S)-1-phenylethylamide diastereomers of the racemic acid followed by treatment with thionyl chloride and then alkaline hydrolysis
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