110169-93-2

Upstream product

• 110079-74-8 N-((E)-1-phenylpent-3-en-2-yl)-N'-phenylurea 
• 42762-51-6 (E)-5-phenyl-3-penten-2-one 
• 99306-80-6 (E)-1-phenylpent-2-en-4-ol 
• 62398-39-4 (E)-1-phenyl-2-aminopent-3-ene 
• 110096-40-7 N-((E)-1-phenylpent-3-en-2-yl)trichloroacetamide 
• 110079-72-6 N-((Z)-1-phenylpent-3-en-2-yl)-N'-phenylurea 
• 6880-16-6 1-phenylpent-3-yn-2-ol 
• 122-78-1 phenylacetaldehyde 
• 110079-65-7 1-phenyl-2-aminopent-3-yne 
• 110079-64-6 1-phenyl-2-phthalimidopent-3-yne 
• 110079-66-8 (Z)-1-phenyl-2-aminopent-3-ene 

Relevant academic research and scientific papers

Stereochemistry of the Epoxidations of Acyclic Allylic Amides. Applications toward the Synthesis of 2,3,6-Trideoxy-3-aminohexoses

The stereochemistry of the epoxidation of several acyclic allylic amides is described.Diastereoselectivity in the (Z)-allylic amide series (compound 1) proved to be dependent both on the amide functionality and epoxidation reagent.The threo epoxide 3 was