110096-40-7

Upstream product

• 42762-51-6 (E)-5-phenyl-3-penten-2-one 
• 99306-80-6 (E)-1-phenylpent-2-en-4-ol 

Downstream Products

• 62398-39-4 (E)-1-phenyl-2-aminopent-3-ene 
• 110169-90-9 N-(xylo-3,4-epoxy-1-phenylpent-2-yl)trichloroacetamide 
• 110169-94-3 N-(lyxo-3,4-epoxy-1-phenylpent-2-yl)trichloroacetamide 
• 110079-73-7 N-carbomethoxy-(E)-1-phenyl-2-aminopent-3-ene 
• 110169-91-0 N-carbomethoxy-xylo-2-amino-3,4-epoxy-1-phenylpentane 
• 110169-92-1 N-carbomethoxy-lyxo-2-amino-3,4-epoxy-1-phenylpentane 
• 110079-74-8 N-((E)-1-phenylpent-3-en-2-yl)-N'-phenylurea 
• 110169-93-2 N-(xylo-3,4-epoxy-1-phenylpent-2-yl)-N'-phenylurea 
• 110170-06-4 1-[(R)-1-((2R,3R)-3-Methyl-oxiranyl)-2-phenyl-ethyl]-3-phenyl-urea 
• 110079-76-0 (R)-1-((4S,5S)-4-Benzyl-2-trichloromethyl-4,5-dihydro-oxazol-5-yl)-ethanol 
• 110169-96-5 <4(R^*,S^*),5(R^*,S^*)-cis>-2-(trichloromethyl)-4-benzyl-5-<1(S^*,R^*)-acetoxyethyl>-2-oxazoline 

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