ALKYLPYRIDINES - EXTENSION OF THE SODAMIDE-LIQUID AMMONIA ALKYLATION METHOD

[1] Salts of the ammono enolic modification of pyridines and quinolines alkylated in the 2-and 4-positions [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1931, 53 : 4065 - 4077

[2] Blaise EE, 1925, CR HEBD ACAD SCI, V180, P1760

[3] A CONVENIENT SYNTHESIS OF THE MONOALKYLPYRIDINES - A NEW PROTOTROPIC REACTION OF 3-PICOLINE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (07) : 3308 - 3312

[4] STERIC EFFECTS IN DISPLACEMENT REACTIONS .3. THE BASE STRENGTHS OF PYRIDINE, 2,6-LUTIDINE AND THE MONOALKYLPYRIDINES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1723 - 1726

[5] CAHOURS A, 1881, COMPT REND, V92, P1082

[6] CHEAVENS TH, 1955, THESIS U TEXAS

[7] Eckert A., 1917, MONATSH CHEM, V38, P225, DOI [10.1007/BF01524213, DOI 10.1007/BF01524213]

[8] Jacobs WA, 1941, J BIOL CHEM, V141, P51

[9] JACOBS WA, 1939, J BIOL CHEM, V129, P79

[10] JACOBS WA, 1942, J BIOL CHEM, V143, P427

[1] Salts of the ammono enolic modification of pyridines and quinolines alkylated in the 2-and 4-positions [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1931, 53 : 4065 - 4077

[2] Blaise EE, 1925, CR HEBD ACAD SCI, V180, P1760

[3] A CONVENIENT SYNTHESIS OF THE MONOALKYLPYRIDINES - A NEW PROTOTROPIC REACTION OF 3-PICOLINE [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (07) : 3308 - 3312

[4] STERIC EFFECTS IN DISPLACEMENT REACTIONS .3. THE BASE STRENGTHS OF PYRIDINE, 2,6-LUTIDINE AND THE MONOALKYLPYRIDINES [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1955, 77 (07) : 1723 - 1726

[5] CAHOURS A, 1881, COMPT REND, V92, P1082

[6] CHEAVENS TH, 1955, THESIS U TEXAS

[7] Eckert A., 1917, MONATSH CHEM, V38, P225, DOI [10.1007/BF01524213, DOI 10.1007/BF01524213]

[8] Jacobs WA, 1941, J BIOL CHEM, V141, P51

[9] JACOBS WA, 1939, J BIOL CHEM, V129, P79

[10] JACOBS WA, 1942, J BIOL CHEM, V143, P427