28557-75-7

Upstream product

• 936-52-7 1-(N-morpholino)cyclopent-1-ene 
• 58321-79-2 (Z)-(2-nitroprop-2-en-1-yl)benzene 
• 120-92-3 cyclopentanone 
• 705-60-2 1-phenyl-2-nitroprop-1-ene 

Downstream Products

• 28612-60-4 4-[5-(2-nitro-1-phenyl-propyl)-cyclopent-1-enyl]-morpholine 
• 83466-02-8 4-[2-(2-Nitro-1-phenyl-propyl)-cyclopent-1-enyl]-morpholine 
• 28612-60-4 4-[(S)-5-((S)-2-Nitro-1-phenyl-propyl)-cyclopent-1-enyl]-morpholine 
• 28612-60-4 4-[(R)-5-((S)-2-Nitro-1-phenyl-propyl)-cyclopent-1-enyl]-morpholine 

Relevant academic research and scientific papers

BICYCLIC 1,2-OXAZINE N-OXIDES. DIFFERENT BEHAVIOUR IN RING FISSION BETWEEN SYSTEMS DERIVED FROM 5- AND 6-MEMBERED RING CYCLIC ENAMINES

1,2-Oxazine N-oxides derived from aminocyclohexenes open into the corresponding nitroalkylated trisubstituted enamines, whereas those derived from aminocyclopentenes give stable tetrasubstituted enamines.Both open-chain systems are easily hydrolyzed to the corresponding χ-nitrocycloalkanones.