109769-57-5

Upstream product

• 455-19-6 4-Trifluoromethylbenzaldehyde 
• 677-22-5 tert-butylmagnesium chloride 
• 312-75-4 trimethyl(4-trifluoromethylphenyl)silane 
• 630-19-3 pivalaldehyde 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 3282-30-2 pivaloyl chloride 
• 329-15-7 4-trifluoromethyl-phenyl acetyl chloride 

Downstream Products

• 120136-24-5 3-Nitro-benzenesulfonic acid 2,2-dimethyl-1-(4-trifluoromethyl-phenyl)-propyl ester 
• 114529-39-4 C₁₂H₁₅F₃O 
• 109837-22-1 C₁₂H₁₅F₃O 
• 586346-65-8 2,2-dimethyl-1-{4-(trifluoromethyl)phenyl}propan-1-one 
• 938-16-9 2,2-dimethylpropiophenone 
• 2040-26-8 1-(4-methoxyphenyl)-2,2-dimethyl-1-propanone 
• 455-19-6 4-Trifluoromethylbenzaldehyde 

Relevant academic research and scientific papers

SUBSTITUTED TRIAZOLO BICYCLICCOMPOUNDS AS PDE2 INHIBITORS

The present invention is directed to substituted triazolo bicycliccompounds of formula (I) which are useful as therapeutic agents for the treatment of central nervous system disorders associated with phosphodiesterase 2 (PDE2). The present invention also

Copper-catalyzed hydrosilylation with a bowl-shaped phosphane ligand: Preferential reduction of a bulky ketone in the presence of an aldehyde

Chemical Equation Presented Hollywood bowl: A highly active copper catalyst with a bowl-shaped phosphane (bsp) ligand was used in the hydrosilylation reaction of bulky ketones. The preferential reduction of a bulky ketone in the presence of an unprotected aldehyde is unprecedented.

Enantioselective hydrogenation and transfer hydrogenation of bulky ketones catalysed by a ruthenium complex of a chiral tridentate ligand

A study on the enantioselective hydrogenation of tertiary alkyl ketones catalysed by a novel class of tridentate-Ru complex is reported. In contrast to the extensively studied [RuCl2(diphos)(di-primary amine)] complexes, this new class of hydro

Phosphazene base-promoted functionalization of aryltrimethylsilanes

The activation of Ar-Si bonds in aryltrimethylsilane was investigated using a catalytic amount of t-Bu-P4 base and selective functionalizations of aryltrimethylsilanes in the absence of strong electron withdrawing groups on the aromatic rings were accomplished. The Royal Society of Chemistry 2006.

CHROMATOGRAPHIC RESOLUTION OF ALKYL ARYL CARBINOLS ON A SILICA-SUPPORTED QUININE CHIRAL STATIONARY PHASE

Several alkyl aryl carbinols can be separated in enantiomers by liquid chromatography upon a new chiral support, prepared by reaction of γ-mercaptopropylsilanized silica with quinine.From the elution order obtained by means of a circular dichroism detecto