53006-28-3

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 54752-30-6 2-p-methylbenzylidene-1-tetralone 

Downstream Products

• 1647159-58-7 1-(trifluoromethylthio)-(E)-(2-(4-methylbenzylidene))-1,2,3,4-tetrahydronaphthalene 
• 1026689-30-4 C₂₃H₂₇NO₂ 
• 1026689-28-0 C₂₅H₂₅NO₂S 
• 1044744-80-0 4-{(3,4-dihydronaphthalen-2-yl)(p-tolyl)methyl}-2,6-dimethylphenol 
• 3042-63-5 β-(4-methylbenzyl)naphthalene 
• 1083314-68-4 C₂₅H₂₄S 

Relevant academic research and scientific papers

Asymmetric Hydrogenation of Racemic Allylic Alcohols via an Isomerization-Dynamic Kinetic Resolution Cascade

Prochiral racemic allylic alcohols are converted to enantioenriched chiral alcohols bearing adjacent stereocenters catalyzed by a diamine diphosphine Ru complex in the presence of tBuOK. The protocol features a broad substrate scope (56 examples) and high

Direct trifluoromethylthiolation of alcohols under mild reaction conditions: Conversion of R-OH into R-SCF3

A direct process for the trifluoromethylthiolation of allylic and benzylic alcohols under mild conditions has been developed. A wide range of free alcohols underwent nucleophilic substitution in the presence of stable CuSCF3 and BF3·Et2O to give the corresponding products in good to excellent yields.