摘要 |
<P>PROBLEM TO BE SOLVED: To provide an advantageous method for producing an optically active compound useful as a synthetic intermediate of a medicine or the like by developing a new nonmetallic asymmetric catalyst capable of achieving high-yield and highly stereoselective asymmetric reaction. <P>SOLUTION: The amino acid derivative is represented by general formula (I) [wherein, R<SP>1</SP>is an aryl group which may have a substituent, a group represented by the formula: -CO<SB>2</SB>R<SP>4</SP>(wherein, R<SP>4</SP>is a hydrogen atom or the like) or the like; and R<SP>2</SP>and R<SP>3</SP>are the same or different and each a hydrogen atom or the like]. The method for producing the optically active compound uses the optically active substance as an asymmetric catalyst. <P>COPYRIGHT: (C)2006,JPO&NCIPI |