Russian chemical bulletin

Reductive desulfurization of 3-cyano-2-methylthiopyridines under the action of Raney nickel

AA Zubarev, VK Zav'yalova, VP Litvinov

Index: Zubarev; Zav'yalova; Litvinov Russian Chemical Bulletin, 2005 , vol. 54, # 11 p. 2578 - 2581

Full Text: HTML

Citation Number: 2

Abstract

Abstract The action of Raney nickel on substituted 3-cyano-2-methylthiopyridines was studied. Under conditions of catalytic hydrogenation, the reaction yields a mixture containing the aminosulfide resulting from reduction of the nitrile group with retention of the methylthio

Related Articles:

The synthesis of some isomeric dimethyl-hydroxymethylpyridines. 3, 4-Didesoxypyridoxin

[Mariella; Leech Journal of the American Chemical Society, 1949 , vol. 71, p. 331]

α-Oxygenated Pyridines. IV. The Synthesis of an Isomer of Pyridoxamine1, 2

[Mariella; Belcher Journal of the American Chemical Society, 1952 , vol. 74, p. 4049]

The synthesis of some isomeric dimethyl-hydroxymethylpyridines. 3, 4-Didesoxypyridoxin

[Mariella; Leech Journal of the American Chemical Society, 1949 , vol. 71, p. 331]

α-Oxygenated Pyridines. IV. The Synthesis of an Isomer of Pyridoxamine1, 2

[Mariella; Belcher Journal of the American Chemical Society, 1952 , vol. 74, p. 4049]

α-Oxygenated Pyridines. IV. The Synthesis of an Isomer of Pyridoxamine1, 2

[Mariella; Belcher Journal of the American Chemical Society, 1952 , vol. 74, p. 4049]

More Articles...