94162-49-9

Upstream product

• 94162-48-8 ((E)-5-Isocyanato-4,4-dimethyl-pent-2-enyloxymethyl)-benzene 
• 75-65-0 tert-butyl alcohol 
• 107-86-8 3,3-dimethyl acrylaldehyde 
• 94162-44-4 4-Methyl-1-(phenylmethoxy)-3-penten-2-ol 
• 94162-45-5 (E)-6-(benzyloxy)-3,3-dimethyl-4-hexenoic acid 
• 86534-20-5 6-(benzyloxy)-3,3-dimethyl-4-hexenoyl chloride 
• 94162-46-6 (E)-6-Benzyloxy-3,3-dimethyl-hex-4-enoic acid ethyl ester 
• 94162-47-7 (E)-6-Benzyloxy-3,3-dimethyl-hex-4-enoyl azide 

Downstream Products

• 94202-33-2 (R)-2-Acetoxy-N-((E)-5-benzyloxy-2,2-dimethyl-pent-3-enyl)-succinamic acid 
• 94162-50-2 (R)-3-Acetoxy-N-((E)-5-benzyloxy-2,2-dimethyl-pent-3-enyl)-succinamic acid 
• 86534-22-7 (+)-4(R)-acetoxy-1-<5-(benzyloxy)-2,2-dimethylpent-3-(E)-en-1-yl>-2,5-pyrrolidinedione 
• 86545-49-5 4(R)-acetoxy-1-<5-(benzyloxy)-2,2-dimethylpent-3(E)-en-1yl>-5-hydroxy-2-pyrrolidinone 
• 86534-21-6 5-(benzyloxy)-2,2-dimethylpent-3(E)-enamine 

Relevant academic research and scientific papers

N-Acyliminium Ion Rearrangements: Generalities and Application to the Synthesis of Pyrrolizidine Alkaloids

N-Acyliminium ions of the 2-aza-1,5-hexadienyl type frequently rearrange to isomeric ions by a process which is formally a 2-aza-Cope rearrangement.When gem-dimethyl substitution is present at C-4 of the initially formed N-acyliminium ion, the rearranged