49684-66-4

Upstream product

• 6295-87-0 N-aminopyridin-1-ium iodide 
• 403-43-0 4-fluorobenzoyl chloride 

Downstream Products

• 1454819-13-6 2,5-bis(4-fluorophenyl)-4-(1H-indol-3-yl)oxazole 
• 1454819-12-5 2-(4-fluorophenyl)-4-(1H-indol-3-yl)-5-phenyloxazole 
• 81460-65-3 N-(3,6-Dihydro-2H-pyridin-1-yl)-4-fluoro-benzamide 

Relevant academic research and scientific papers

Highly regioselective synthesis of 2,4,5-(hetero)aryl substituted oxazoles by intermolecular [3+2]-cycloaddition of unsymmetrical internal alkynes

A robust N-nucleophilic 1,3-N,O-dipole equivalent reacts with unsymmetrical internal alkynes under gold catalysis. Conjugation from a remote nitrogen lone pair enables and controls this convergent and highly regioselective process.

Synthesis of N-[[(substituted-phenyl)carbonyl]amino]-1,2,3,6-tetrahydropyridines with analgesic and hyperglycemic activity

A group of N-[(phenylcarbonyl)amino]-1,2,3,6-tetrahydropyridines, 5, were synthesized to determine the effect that changes in aromatic substitution on the phenyl ring have on analgesic, hyperglycemic, and antiinflammatory activities. All of the N-[(phenyl