227030-66-2

Upstream product

• 773837-37-9 sodium cyanide 
• 7730-39-4 N-benzyl azetidine 
• 104-63-2 N-Benzylethanolamine 
• 154582-42-0 [benzyl-(2-hydroxyethyl)-amino]-acetonitrile 
• 928056-21-7 [benzyl-(2-chloroethyl)-amino]-acetonitrile 

Downstream Products

• 142301-75-5 N-(tert-butoxycarbonyl)-N-benzyl-4-amino-1-butyne 
• 107301-61-1 N-benzyl-4-amino-1-butyne 
• 1393814-44-2 2-benzyl-5-cyano-isoxazolidine 
• 1393814-43-1 C₁₁H₁₄N₂O₂ 
• 1269461-10-0 C₁₅H₂₁NO 
• 205443-26-1 (S)-(-)-1-benzylazetidine-2-carboxamide 
• 1179838-75-5 (S)-1-benzylazetidine-2-carbonitrile 
• 209607-00-1 (R)-1-benzylazetidine-2-carboxamide 

Relevant academic research and scientific papers

RuO4-mediated oxidation of N-benzylated tertiary amines. Four- And three-membered azacycloalkanes as substrates

Similarly to N-benzylpiperidine and -pyrrolidine, N-benzylazetidine underwent RuO4-catalyzed oxidation by attack at both types of N-methylene C-H bonds: Endocyclic and exocyclic (benzylic). If the reaction is performed in the presence of cyanide, α-aminon

Strained azetidinium ylides: New reagents for cyclopropanation

(Chemical Equation Presented) Azetidinium ylides showed a remarkable ability to perform the cyclopropanation of Michael acceptors. Ephedrine-derived azetidinium ylides allowed the formation of substituted cyclopropanes in good yields and at a high level o