16196-92-2Relevant academic research and scientific papers
Organocatalyzed and mechanochemical solvent-free synthesis of novel and functionalized bis-biphenyl substituted thiazolidinones as potent tyrosinase inhibitors: SAR and molecular modeling studies
Mutahir, Sadaf,Khan, Muhammad Asim,Khan, Islam Ullah,Yar, Muhammad,Ashraf, Muhammad,Tariq, Sidra,Ye, Ren-long,Zhou, Bao-jing
, p. 406 - 414 (2017)
Eluding the involvement of solvents in organic synthesis and introducing environment friendly procedures can control environmental problems. A facile and an efficient solvent free mechanochemical method (grinding) is achieved to synthesize novel bis-biphe
Synthesis and spectroscopic studies of some new oxazepine derivatives throughout [2+5] cycloaddition reactions (III)
Mahrath, Alaa J.,Aowda, Saadon A.,Kamil, Sabah N.
, p. 3739 - 3752 (2013/10/22)
The present work included condensation reactions of o-tolidine with different aromatic aldehydes in absolute ethanol to give Schiff bases (w 9 -w 12 ) in high yield which, on reaction with maleic and phthalic anhydride by [2+5] cycloaddition reactions in the presence of suitable solvents, give the corresponding [1,3]oxazepine-4,7-dione (w 9 m-w 12 m) and [1,3]oxazepine-1,5-dione (w 9 ph-w 12 ph), respectively. The structure of the newly synthesized compounds were monitored by TLC and established on the basis of elemental analysis, FT-IR, and 1H NMR.
Characteristic and spectroscopic properties of the Schiff-base model compounds
Jarzabek,Kaczmarczyk,Sek
experimental part, p. 949 - 954 (2010/03/30)
Two series of conjugated aromatic imines (Schiff-base model compounds) with different central groups and various side-group substitutions have been synthesized and characterized by elemental analysis, differential scanning calorimetry (DSC) technique, hyd
