Thin-layer chromatographic separation of some sulpha drugs using acetoacetanilide as a coupling agent.
R Jain, A Bhatia
Index: J. Chromatogr. A. 441(2) , 454-7, (1988)
Full Text: HTML
Abstract
Related Articles:
Kinetics and mechanisms of reactions between H2O2 and copper and copper oxides.
2015-09-28
[Dalton Trans. 44 , 16045-51, (2015)]
Acetoacetanilides as masked isocyanates: facile and efficient synthesis of unsymmetrically substituted ureas.
2010-10-01
[Org. Lett. 12 , 4220-4223, (2010)]
Massive screening yields novel and selectiveTrypanosoma cruzitriosephosphate isomerase dimer-interface-irreversible inhibitors with anti-trypanosomal activity
2010-01-01
[Eur. J. Med. Chem. 45 , 5767-72, (2010)]
FeCl3⋅6H2O-catalyzed intermolecular-cascade cyclization of acetoacetanilide: aldehyde-tuned synthesis to valuable 2-pyridone analogues.
2012-02-13
[Chemistry 18(7) , 1905-9, (2012)]
Regiospecific β-lactam ring-opening/recyclization reactions of N-aryl-3-spirocyclic-β-lactams catalyzed by a Lewis-Brønsted acids combined superacid catalyst system: a new entry to 3-spirocyclicquinolin-4(1H)-ones.
2012-01-18
[Chem. Commun. (Camb.) 48(5) , 690-2, (2012)]