118485-45-3

Upstream product

• 606-83-7 3,3-Diphenylpropionic acid 
• 1666-17-7 benzaldehyde p-toluenesulfonylhydrazone 
• 1258504-63-0 2-iodo-4'-methoxychalcone 
• 2142-70-3 2-iodoacetophenone 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 1254271-32-3 (E)-1-(2-iodophenyl)-3-(4-methoxyphenyl)prop-2-en-1-one 
• 37089-77-3 3,3-diphenylpropanoyl chloride 
• 16618-72-7 3-phenyl-1-indanone 
• 123-11-5 4-methoxy-benzaldehyde 

Downstream Products

• 118485-31-7 C₃₆H₂₈N₂O₂ 
• 118485-33-9 C₃₆H₂₇N₃O₄ 
• 118485-32-8 C₃₇H₃₀N₂O₂ 

Relevant academic research and scientific papers

Phosphine-Free and Reusable Palladium Nanoparticles-Catalyzed Domino Strategy: Synthesis of Indanone Derivatives

The carbene migratory insertion involving a domino reaction by highly stable, reusable, and binaphthyl-stabilized Pd-nanoparticles (Pd-BNP) is disclosed. The reaction was catalyzed by 2 mol % of a heterogeneous Pd-BNP catalyst under external ligand-free c

Palladium-Catalyzed Intermolecular Carbene Insertion Prior to Intramolecular Heck Cyclization: Synthesis of 2-Arylidene-3-aryl-1-indanones

A domino process that converges the migratory insertion of carbene with a Heck reaction has been established as a versatile tool for the synthesis of 2-arylidene-3-aryl-1-indanones from very stable and easily accessible N-tosylhydrazones and 2′-iodochalco

Synthesis, characterization, biological evaluation and QSAR studies of 11-p-substituted phenyl-12-phenyl-11a,12-dihydro-11H-indeno[2,1-c][1,5] benzothiazepines as potential antimicrobial agents

A novel series of 11-p-substituted phenyl-12-phenyl-11a,12-dihydro-11H- indeno[2,1-c][1,5]benzothiazepines (3) has been synthesized and screened for their antimicrobial activity against Gram-positive (Bacillus subtilis and Staphylococcus aureus) and Gram-negative (Escherichia coli and Pseudomonas aeruginosa) bacteria and fungi (Aspergillus fumigates and Candida albicans). The antimicrobial evaluation data indicated that the compounds, 3d, 3g, 3h, 3k-3p exhibited very promising antibacterial activity and the derivatives 3k, 3l, 3o and 3p exhibited high antifungal activity. The QSAR studies carried out to find out the correlation between the antimicrobial activity and physicochemical properties of synthesized benzothiazepines (3) indicated the predominance of electronic parameters in describing their antimicrobial activity.