THE ALKYLATION OF MALONIC ESTER

[1] The disposition of the bonds of the quinquevalent nitrogen atom Part I [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1915, 107 : 887 - 902

[2] CONRAD, 1921, Z PHYSIK CHEM, V99, P116

[3] The degree of ionization of ethyl alcohol II From measurements of electromotive force [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1922, 44 : 2832 - 2841

[4] GOLDSCHMIDT, 1921, Z PHYS CHEM, V99, P116

[5] The malonic ester synthesis and Walden inversion [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1942, 64 : 2606 - 2610

[6] A better representation of mono substituted malonester and acetic ester [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1911, 44 : 1507 - 1511

[7] MANSKE RH, 1931, J AM CHEM SOC, V53, P1106

[8] MECHANISM OF THE ACETOPHENONE IODINE PYRIDINE REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1947, 69 (12) : 3100 - 3103

[9] 1941, ORGANIC SYNTHESES, V1, P250

[1] The disposition of the bonds of the quinquevalent nitrogen atom Part I [J]. JOURNAL OF THE CHEMICAL SOCIETY, 1915, 107 : 887 - 902

[2] CONRAD, 1921, Z PHYSIK CHEM, V99, P116

[3] The degree of ionization of ethyl alcohol II From measurements of electromotive force [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1922, 44 : 2832 - 2841

[4] GOLDSCHMIDT, 1921, Z PHYS CHEM, V99, P116

[5] The malonic ester synthesis and Walden inversion [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1942, 64 : 2606 - 2610

[6] A better representation of mono substituted malonester and acetic ester [J]. BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1911, 44 : 1507 - 1511

[7] MANSKE RH, 1931, J AM CHEM SOC, V53, P1106

[8] MECHANISM OF THE ACETOPHENONE IODINE PYRIDINE REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1947, 69 (12) : 3100 - 3103

[9] 1941, ORGANIC SYNTHESES, V1, P250