A novel synthesis of optically active alpha-amino acids

1997-01-01
Demir, Ayhan Sıtkı
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A new enantioselective synthesis of alpha- amino acids are described in which the key step is the enantioselective reduction of E, and Z furyl ketone oxime ethers with chiral boron complexes. The chirality of amino acid is fully controlled by appropriate choice of geometrical isomer of the oxime ether.
General Chemistry, General Chemical Engineering
https://hdl.handle.net/11511/57241
PURE AND APPLIED CHEMISTRY
Department of Chemistry, Article

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Citation Formats
A. S. Demir, “A novel synthesis of optically active alpha-amino acids,” PURE AND APPLIED CHEMISTRY, pp. 105–108, 1997, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/57241.
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