[1]
|
Voet, D. and Voet, J.G. (2010) Biochemistry. 4th Edition, Wiley, Hoboken.
|
[2]
|
McMurry, J.E. and Begley, T.P. (2005) The Organic Chemistry of Biological Pathways. Roberts and Company Publishers, Englewood.
|
[3]
|
Zimmerman, S.C. and Breslow, R. (1984) Asymmetric Synthesis of Amino Acids by Pyridoxamine Enzyme Analogs Utilizing General Base-Acid Catalysis. Journal of the American Chemical Society, 106, 1490-1491. http://dx.doi.org/10.1021/ja00317a054
|
[4]
|
Michael, B.S. and March, J. (2007) March’s Advanced Organic Chemistry. 6th Edition, John Wiley & Son, Inc., Hoboken.
|
[5]
|
Harada, K. and Munegumi, T. (1991) Reduction of C=X to CHXH by Catalytic Hydrogenation. In: B. M. Trost and I. Fleming, Eds., Comprehensive Organic Synthesis, Elsevier Science Ltd., Oxford, 139-158. http://dx.doi.org/10.1016/B978-0-08-052349-1.00222-5
|
[6]
|
Matsumoto, K. and Harada, K. (1966) Stereoselective Syntheses of Optically Active Amino Acids from Menthyl Esters of α-Keto Acids. Journal of Organic Chemistry, 31, 1956-1958. http://dx.doi.org/10.1021/jo01344a064
|
[7]
|
Harada, K. and Matsumoto, K. (1967) Sterically Controlled Syntheses of Optically Active Organic Compounds. V. Sterically Controlled Synthesis of Optically Active α-Amino Acids from α-Keto Acids by Reductive Amination. Journal of Organic Chemistry, 32, 1794-1800. http://dx.doi.org/10.1021/jo01281a020
|
[8]
|
Harada, K. and Matsumoto, K. (1968) Sterically Controlled Syntheses of Optically Active Organic Compounds. VI. Solvent Effect in a Sterically Controlled Synthesis of Optically Active α-Amino Acids from α-Keto Acids by Hydrogenolytic Asymmetric Transamination. Journal of Organic Chemistry, 33, 4467-4470. http://dx.doi.org/10.1021/jo01276a036
|
[9]
|
Harada, K. and Yoshida, T. (1970) A Temperature Effect in an Asymmetric Synthesis by Hydrogenolytic Asymmetric Transamination. Journal of the Chemical Society D: Chemical Communications, 1970, 1071-1072. http://dx.doi.org/10.1039/c29700001071
|
[10]
|
Harada, K. and Yoshida, T. (1970) Syntheses of Optically Active α-Amino Acids from Esters of α-Keto Acids by Hydrogenolytic Asymmetric Transamination, a Solvent Effect. Bulletin of the Chemical Society of Japan, 43, 921-925. http://dx.doi.org/10.1246/bcsj.43.921
|
[11]
|
Harada, K. and Matsumoto, K. (1971) Sterically Controlled Syntheses of Optically Active Organic Compounds. XIV. Syntheses of Dipeptides from N-(α-Ketoacyl)-α-Amino Acid Esters. Bulletin of the Chemical Society of Japan, 44, 1068-1071. http://dx.doi.org/10.1246/bcsj.44.1068
|
[12]
|
Harada, K. and Kataoka, Y. (1978) Asymmetric Synthesis of Alanine by Hydrogenolytic Asymmetric Transamination. Tetrahedron Letters, 19, 2103-2106. http://dx.doi.org/10.1016/S0040-4039(01)94761-6
|
[13]
|
Harada, K. and Kataoka, Y. (1978) The Temperature Dependence of Hydrogenolytic Asymmetric Transamination between Esters of Optically Active Phenylglycine and Pyruvic Acid. Chemistry Letters, 7, 791-794. http://dx.doi.org/10.1246/cl.1978.791
|
[14]
|
Harada, K. and Tamura, M. (1979) Asymmetric Synthesis of Alanine by Hydrogenolytic Asymmetric Transamination between (R)-2-Amino-2-Phenylethanol and Ethyl Pyruvate. Bulletin of the Chemical Society of Japan, 52, 1227-1228. http://dx.doi.org/10.1246/bcsj.52.1227
|
[15]
|
Harada, K., Munegumi, T. and Nomoto, S. (1981) Asymmetric Hydrogenation of Chiral Pyruvamides. Tetrahedron Letters, 22, 111-114. http://dx.doi.org/10.1016/0040-4039(81)80162-1
|
[16]
|
Harada, K. and Munegumi, T. (1983) Asymmetric Hydrogenations of N-Pyruvoyl-(S)-Amino Acids Esters. Bulletin of the Chemical Society of Japan, 56, 2774-2777. http://dx.doi.org/10.1246/bcsj.56.2774
|
[17]
|
Harada, K. and Munegumi, T. (1984) Asymmetric Catalytic Hydrogenations of Chiral α-Keto Amides. Bulletin of the Chemical Society of Japan, 57, 3203-3232. http://dx.doi.org/10.1246/bcsj.57.3203
|
[18]
|
Munegumi, T., Fujita, M., Maruyama, T., Shiono, S., Takasaki, M. and Harada, K. (1987) Asymmetric Catalytic Hydrogenation of N-Pyruvoyl-(S)-Proline Esters. Bulletin of the Chemical Society of Japan, 60, 249-253. http://dx.doi.org/10.1246/bcsj.60.249
|
[19]
|
Munegumi, T. and Harada, K. (1988) Asymmetric Catalytic Hydrogenations of Oximes and Benzylimino Derivatives of Chiral Pyruvamides. Bulletin of the Chemical Society of Japan, 61, 1425-1427. http://dx.doi.org/10.1246/bcsj.61.1425
|
[20]
|
Munegumi, T., Maruyama, T., Takasaki, M. and Harada, K. (1990) Diastereoselective Catalytic Hydrogenations of Nα-Pyruvoyl-(S)-Prolinamide. Bulletin of the Chemical Society of Japan, 63, 1832-1834. http://dx.doi.org/10.1246/bcsj.63.1832
|
[21]
|
Dorman, D.E. and Bovery, F.A. (1973) Carbon-13 Magnetic Resonance Spectroscopy. Spectrum of Proline in Oligopeptides. Journal of Organic Chemistry, 38, 2379-2383. http://dx.doi.org/10.1021/jo00953a021
|
[22]
|
Osawa, M., Hatta, A., Harada, K. and Suetaka, W. (1976) Infrared Dichroism and Molecular Orientation of Ethyl 2-Hydroxyimino-3-Oxo-3-Phenylpropinate in Thin Films on Pd Metal Surfaces. Bulletin of the Chemical Society of Japan, 49, 1512-1516. http://dx.doi.org/10.1246/bcsj.49.1512
|