Properties of sodium bis(2-methoxyethoxy)aluminium hydride. IX. Reduction and hydrogenolysis of amino-substituted aromatic aldehydes, ketones, carboxylic acids, esters, and carbinols

1970 ◽  
Vol 35 (4) ◽  
pp. 1216-1223 ◽  
Author(s):  
M. Černý ◽  
J. Málek
2018 ◽  
Vol 21 (4) ◽  
pp. 298-301 ◽  
Author(s):  
Ghasem Marandi

Aim and Objective: The reaction of cyclohexylisocyanide and 2-aminopyridine-3- carboxylic acid in the presence of benzaldehyde derivatives in ethanol led to 3-(cyclohexylamino)-2- arylimidazo[1,2-a]pyridine-8-carboxylic acids in high yields. In a three component condensation reaction, isocyanide reacts with 2-aminopyridine-3-carboxylic acid and aromatic aldehydes without any prior activation. Material and Methods: The synthesized products have stable structures which have been characterized by IR, 1H, 13C and Mass spectroscopy as well as CHN-O analysis. Results: In continuation of our attempts to develop simple one-pot routes for the synthesis of 3- (cyclohexylamino)-2-arylimidazo[1,2-a]pyridine-8-carboxylic acids, aromatic aldehydes with divers substituted show a high performance. Conclusion: In conclusion, this study introduces the art of combinatorial chemistry using a simple one-pot procedure for the synthesis of new materials which are interesting compounds in medicinal and biological sciences.


2004 ◽  
Vol 26 (21) ◽  
pp. 1643-1648 ◽  
Author(s):  
Koichi Mitsukura ◽  
Yukihide Sato ◽  
Toyokazu Yoshida ◽  
Toru Nagasawa

2016 ◽  
Vol 40 (12) ◽  
pp. 715-717 ◽  
Author(s):  
Negar Moshref Javadi ◽  
Javad Azizian

A series of new 6-(4-carboxy-3-methyl-2-phenylquinolin-6-ylsulfonyl)-3-methyl-2-phenylquinoline-4-carboxylic acids were synthesised by a one-pot reaction of dapsone, α-ketobutyric acid, and aromatic aldehydes in the presence of CuBr2 as a catalyst. Operational simplicity, mild reaction conditions, and eco-friendly procedure make this novel protocol a promising alternative for the preparation of quinoline-4-caboxylic acid derivatives. The structures of the products were established by elemental analyses and spectroscopic data. The biological activity of the new sulfone dimers was evaluated as having the potential for use as anticancer agents.


2016 ◽  
Vol 48 (3) ◽  
pp. 413-417 ◽  
Author(s):  
N. F. L. Machado ◽  
M. P. M. Marques ◽  
L. A. E. Batista de Carvalho ◽  
J. L. Castro ◽  
J. C. Otero

2015 ◽  
Vol 1 (2) ◽  
pp. e1500020 ◽  
Author(s):  
Mingxin Liu ◽  
Haining Wang ◽  
Huiying Zeng ◽  
Chao-Jun Li

The first example of a homogeneous silver(I)-catalyzed aerobic oxidation of aldehydes in water is reported. More than 50 examples of different aliphatic and aromatic aldehydes, including natural products, were tested, and all of them successfully underwent aerobic oxidation to give the corresponding carboxylic acids in extremely high yields. The reaction conditions are very mild and greener, requiring only a very low silver(I) catalyst loading, using atmospheric oxygen as the oxidant and water as the solvent, and allowing gram-scale oxidation with only 2 mg of our catalyst. Chromatography is completely unnecessary for purification in most cases.


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