65609-77-0

Upstream product

• 141-97-9 ethyl acetoacetate 
• 4224-96-8 3-phenyl-1-p-tolylprop-2-en-1-one 
• 1007476-32-5 sodium ethyl acetylacetate enolate 

Downstream Products

• 1097646-33-7 6-(p-tolyl)-4-phenyl-4,5-dihydro-2H-indazol-3-ol 
• 1161082-28-5 2,4-diphenyl-6-(p-tolyl)-4,5-dihydro-2H-indazol-3-ol 
• 65609-82-7 3-(4'-methylphenyl)-5-phenylcyclohexenone 
• 1190880-53-5 C₂₂H₂₁NO₂ 

Relevant academic research and scientific papers

A highly efficient metal-free approach to: Meta - And multiple-substituted phenols via a simple oxidation of cyclohexenones

A novel and efficient metal-free approach to substituted phenols has been disclosed from simple and readily available cyclohexenones and cyclohexenone equivalents. Dimethyl sulfoxide (DMSO), a simple and common organic reagent, was employed as a mild oxidant in this I2-catalysis, which significantly tolerates various substituents including some easily oxidizable or reducible functionalities. The challenging meta- and multiple-substituted phenols could be well prepared by this method. The metal-free and mild oxidation make this protocol very simple, practical, and easy to handle.

Microwave assisted rapid and efficient. synthesis of new 3-ethoxy-4,6-diaryl-4,5- Dihydro-2,1-benzisoxazoles

A simple, extremely fast and efficient synthesis of new 3- ethoxy-4,6-diaryl-4,5-dihydro2,l-benzisoxazoles has been achieved under microwave irradiation.

Synthesis and characterization of 4,6-diaryl-4,5-dihydro-2H-indazol-3-ols and 4,6-diaryl-2-phenyl-4,5-dihydro-2H-indazol-3-ols - A new series of fused indazole derivatives

A novel class of 4,6-diaryl-4,5-dihydro-2H-indazol-3-ols and 4,6-diaryl-2-phenyl-4,5-dihydro-2H-indazol-3-ols is synthesized and characterized by melting point, elemental analysis, MS, FT-IR, 1H and 13C NMR, D2O exchanged 1H NMR, and two-dimensional HSQC spectra.