110079-73-7

Upstream product

• 1189-71-5 isocyanate de chlorosulfonyle 
• 42762-51-6 (E)-5-phenyl-3-penten-2-one 
• 110096-40-7 N-((E)-1-phenylpent-3-en-2-yl)trichloroacetamide 
• 139239-48-8 (+/-)-(E)-1-phenyl-3-penten-2-ol 
• 99306-80-6 (E)-1-phenylpent-2-en-4-ol 
• 62398-39-4 (E)-1-phenyl-2-aminopent-3-ene 
• 79-22-1 methyl chloroformate 

Downstream Products

• 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 

Relevant academic research and scientific papers

Synthesis of N-protected allylic amines from allyl ethers

A synthetic method for N-protected allylic amines from allyl ethers using chlorosulfonyl isocyanate (CSI) is presented. The reaction of 4-phenylbut-2-enyl methyl ether (1i) with CSI afforded methyl N-(1-benzylallyl)carbamate (2i) and methyl N-(4-phenylbut

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