144119-16-4Relevant academic research and scientific papers
1,3-Diphenylpyrazoles: Synthesis and antiparasitic activities of azomethine derivatives
Rathelot, Pascal,Azas, Nadine,El-Kashef, Hussein,Delmas, Florence,Di Giorgio, Carole,Timon-David, Pierre,Maldonado, José,Vanelle, Patrice
, p. 671 - 679 (2002)
1,3-Diphenylpyrazole-4-carboxaldehyde and 1-(4-nitrophenyl)-3-phenylpyrazole-4-carboxaldehyde were obtained from the appropriated phenylhydrazones via the Vilsmeier-Haack reaction. These two aldehydes were functionalized by various substituted anilines or substituted benzylamines. Antiparasitic activities of the corresponding azomethines were assessed. In the most cases, nitrated compounds were found to be more efficient than non-nitrated ones against Plasmodium falciparum, Trichomonas vaginalis and Leishmania infantum.
Synthesis, Reactions and Antitumor Activity of Certain 1,3-diphenylpyrazole-4-carboxaldehyde Derivatives
Amer, Atef M.,Ramses, Neveen,Mahgoub, Sebaey
, p. 51 - 65 (2019/03/28)
IN activity continuation especially of our the interest antitumor in synthesis activity.In of novel this paper heterocycles we have with discussed anticipat
Synthesis of 1,3-diphenylpyrazoles with substituted thiazolidinone, Δ2-1,2,4-oxadiazoline, Δ2-pyrazoline or Δ2-isoxazoline moiety at position-4
Chary, T Jagan Mohana,Reddy, Ch V Narsimha,Murthy, A Krishna
, p. 495 - 498 (2007/10/02)
The schiff bases (1) obtained from 1,3-diphenylpyrazole-4-aldehyde and anilines have been converted into thiazolidinones (2) and Δ2-oxadiazolines (3) by interaction with mercaptoacetic acid and benzonitrile oxide respectively.The propenones (4)
