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AXIAL-ASYMMETRIC N-(2-ACYLARYL)-2-5, 7-DIHYDRO-6H-DIBENZO C, E AZEPINE-6-YL ACETAMIDE COMPOUND AND CHIRALITY CONVERSION METHOD FOR Α-AMINO ACID USING SAME
AXIAL-ASYMMETRIC N-(2-ACYLARYL)-2-5, 7-DIHYDRO-6H-DIBENZO C, E AZEPINE-6-YL ACETAMIDE COMPOUND AND CHIRALITY CONVERSION METHOD FOR Α-AMINO ACID USING SAME
The present invention addresses the problem of providing: a production method capable of high-yield/high-enantioselectively producing an optically active amino acid having few restrictions on the material that can be used as the substrate therefor; and a useful compound, as a chiral auxiliary agent; etc. The present invention provides an N-(2-acylaryl)-2-[5, 7-dihydro-6H-dibenzo [c, e] azepine-6-yl] acetamide compound indicated in formula (1), a salt thereof, or a metal complex indicated in formula (3).
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