858823-61-7

Upstream product

• 1504-58-1 3-Phenyl-2-propyn-1-ol 
• 456-27-9 4-nitrobenzenediazonium tetrafluoroborate 
• 50-00-0 formaldehyd 
• 3769-82-2 2-(4-nitrophenyl)-1-phenylethanone 

Downstream Products

• 116375-70-3 3-(Hydroxy-methyl-amino)-2-(4-nitro-phenyl)-1-phenyl-propan-1-one 
• 116375-67-8 3-(tert-Butyl-hydroxy-amino)-2-(4-nitro-phenyl)-1-phenyl-propan-1-one 
• 116375-68-9 3-(Cyclohexyl-hydroxy-amino)-2-(4-nitro-phenyl)-1-phenyl-propan-1-one 
• 116375-84-9 C₄₂H₄₂N₄O₈ 
• 116375-86-1 [(3S,6S)-6-Benzoyl-1,4-dibenzyl-3,6-bis-(4-nitro-phenyl)-tetrahydro-isoxazolo[4,3-c]isoxazol-3-yl]-phenyl-methanone 
• 116375-87-2 [(3S,6S)-6-Benzoyl-1,4-dimethyl-3,6-bis-(4-nitro-phenyl)-tetrahydro-isoxazolo[4,3-c]isoxazol-3-yl]-phenyl-methanone 
• 116375-69-0 3-(Benzyl-hydroxy-amino)-2-(4-nitro-phenyl)-1-phenyl-propan-1-one 

Relevant academic research and scientific papers

Domino Meyer-Schuster/Arylation Reaction of Alkynols or Alkynyl Hydroperoxides with Diazonium Salts Promoted by Visible Light under Dual Gold and Ruthenium Catalysis

A method for the arylative coupling of alkynols or alkynyl hydroperoxides using equimolar amounts of diazonium salts at room temperature has been achieved through application of a gold/photoredox dual catalytic system. The excess of external reagents (oxi

Three Step Synthesis of Fully and Differently Arylated Pyridines

Condensation of β-(2-pyridyl)enamine and α,β-unsaturated ketone in the presence of FeCl3 under air afforded highly substituted pyridines. In this transformation, FeCl3 acted as not only an acid catalyst but also an oxidant for the in