THE STEREOCHEMISTRY OF HYDROXYPROLINE

[21] KREBS HA, 1939, ENZYMOLOGIA, V7, P53

[22] KUHN, 1928, BER, V61, P508

[23] LEUCHS, 1905, BER, V38, P1907

[24] Representation of the three stereoisomeric shapes with natural oxi-prolin. (On pyrrolidin-derivatives, V.) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1919, 52 : 2086 - 2097

[25] The synthesis of natural oxy-proline (on pyrrolidine-derivatives IV) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1913, 46 : 986 - 1000

[26] A new method for the application of optically active alpha-amino acids for both the right and left handed sides (II. Communication) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1931, 64 : 1221 - 1232

[27] On a new method for appropriation of optically-active alpha-amino acids of the right series or left series (I. Announcement.). [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1930, 63 : 448 - 460

[28] MCKENZIE, 1922, J CHEM SOC, V121, P1348

[29] The conversion of malonic acid into d-malic acid. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1923, 123 : 1090 - 1096

[30] PURDIE, 1910, J CHEM SOC, V97, P1517

[21] KREBS HA, 1939, ENZYMOLOGIA, V7, P53

[22] KUHN, 1928, BER, V61, P508

[23] LEUCHS, 1905, BER, V38, P1907

[24] Representation of the three stereoisomeric shapes with natural oxi-prolin. (On pyrrolidin-derivatives, V.) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1919, 52 : 2086 - 2097

[25] The synthesis of natural oxy-proline (on pyrrolidine-derivatives IV) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1913, 46 : 986 - 1000

[26] A new method for the application of optically active alpha-amino acids for both the right and left handed sides (II. Communication) [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1931, 64 : 1221 - 1232

[27] On a new method for appropriation of optically-active alpha-amino acids of the right series or left series (I. Announcement.). [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1930, 63 : 448 - 460

[28] MCKENZIE, 1922, J CHEM SOC, V121, P1348

[29] The conversion of malonic acid into d-malic acid. [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1923, 123 : 1090 - 1096

[30] PURDIE, 1910, J CHEM SOC, V97, P1517