936240-33-4

Upstream product

• 936240-32-3 4-oxy-1,4-diaza-spiro[4.5]dec-3-en-2-one 
• 100-39-0 benzyl bromide 
• 19718-88-8 1,4-diazaspiro[4,5]decan-2-one 
• 19811-52-0 Boc-glycine-benzylamide 
• 1438895-38-5 C₁₅H₂₀N₂O 
• 108-94-1 cyclohexanone 

Downstream Products

• 1438895-37-4 C₁₅H₁₇ClN₂O 
• 1438895-19-2 1-benzyl-3-phenyl-1,4-diazaspiro[4.5]dec-3-en-2-one 
• 1438895-20-5 C₂₁H₂₁FN₂O 
• 1438895-21-6 C₂₁H₂₁FN₂O 
• 1438895-22-7 C₂₁H₂₁FN₂O 
• 1438895-23-8 C₂₁H₂₀F₂N₂O 
• 1438895-24-9 C₂₂H₂₄N₂O 
• 1438895-25-0 C₂₂H₂₄N₂O 
• 1438895-26-1 C₂₂H₂₄N₂O 
• 1438895-27-2 C₂₂H₂₄N₂O₂ 
• 1438895-28-3 C₂₂H₂₄N₂O₂ 
• 1438895-29-4 C₂₂H₂₄N₂O₂ 
• 1438895-30-7 C₂₃H₂₆N₂O₃ 
• 1438895-31-8 C₂₀H₂₁N₃O 

Relevant academic research and scientific papers

A novel method for the preparation of 4-arylimidazolones

A series of 4-arylimidazolones have been accessed via late-stage, palladium-mediated arylation of acetone- and cyclohexanone-derived 4-chloroimidazolones. The 4-chloroimidazolones were prepared via a novel rearrangement of the corresponding imidazolone N-

Versatile spirocyclic glycine-based nitrones and their highly stereoselective 1,3-dipolar cycloaddition

A convenient and efficient method for the synthesis of novel spirocyclic nitrones prepared from glycine derivatives is reported. The 1,3-cycloaddition reactions of the nitrones with alkenes lead to novel isoxazolidines in high yields and with excellent re