38661-89-1

Upstream product

• 110-89-4 piperidine 
• 103-79-7 1-phenyl-acetone 
• 104-87-0 4-methyl-benzaldehyde 
• 1794-48-5 1-bromo-3-phenylprop-2-yne 
• 319923-28-9 C₁₇H₁₆O 

Downstream Products

• 96633-24-8 3-phenyl-4-p-tolyl-6-methyl-5-hepten-2-one 
• 96633-23-7 3-phenyl-3-(phenylseleno)-4-p-tolyl-6-methyl-5-hepten-2-one 
• 96633-34-0 1-phenyl-2-methyl-3-p-tolylcyclopropene 
• 181695-90-9 4-[3-methyl-5-(4-methylphenyl)isoxazol-4-yl]benzenesulfonamide 
• 96633-33-9 3-phenyl-4-p-tolylbuten-2-one tosylhydrazone 

Relevant academic research and scientific papers

Acid-catalyzed synthesis of α,β-disubstituted conjugated enones by a Meyer-Schuster-type rearrangement in allenols

A novel, direct and simple methodology to gain access to α,β-disubstituted conjugated enones from α-allenols in a sustainable metal catalysis context, considering the inexpensiveness and environmentally friendliness of iron(III) species and protons, has b

Iridium-catalyzed asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones: Enantioselective total synthesis of (-)-mesembrine

A highly efficient asymmetric hydrogenation of α-substituted α,β-unsaturated acyclic ketones catalyzed by chiral spiro iridium complexes for the preparation of chiral 2-substituted allylic alcohols has been developed (ee up to 99.7%). This method provides a concise route to (-)-mesembrine (34% yield, 12 steps).

Isoxazole compounds as cyclooxygenase inhibitors

A class of substituted isoxazolyl compounds is described for use in treating cyclooxygenase-2 related disorders. Compounds of particular interest are defined by Formula I STR1 wherein R1, R2, and R3, are described in the specification.