1269460-89-0

Upstream product

• 39149-80-9 tert-butyl 2-bromopropionate 
• 104-63-2 N-Benzylethanolamine 

Downstream Products

• 1269460-95-8 C₁₆H₂₄ClNO₂ 
• 1269460-98-1 C₁₆H₂₃NO₂ 
• 1269460-63-0 C₁₂H₁₇NO 
• 1363402-35-0 2-methylazetidine-1,2-dicarboxylic acid 1-tert-butyl ester 
• 1384745-52-1 (R)-2-methyl-azetidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester 
• 1384745-48-5 (S)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester 
• 1384745-44-1 (1S,2S)-2-(2-hydroxy-1-phenyl-ethylcarbamoyl)-2-methylazetidine-1-carboxylic acid benzyl ester 
• 1384745-41-8 (1S,2R)-(9H-fluoren-9-yl)methyl 2-(2-hydroxy-1-phenylethylcarbamoyl)-2-methylazetidine-1-carboxylate 
• 1384745-37-2 (1S,2S)-(9H-fluoren-9-yl)methyl 2-(2-hydroxy-1-phenylethylcarbamoyl)-2-methylazetidine-1-carboxylate 
• 1179839-12-3 (R)-1-benzyl-2-methyl-azetidine-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Practical preparation of enantiopure 2-methyl-azetidine-2-carboxylic acid; a γ-turn promoter

A robust and practical synthesis of each enantiomer of 2-methyl-azetidine- 2-carboxylic acid, based on the use of (S)-phenylglycinol as resolving agent, is described. This synthesis affords practical quantities of this quaternary amino acid suitably N- an

Ring expansion of 2-(1-Hydroxyalkyl)azetidines to 4-(2-Chloroethyl) oxazolidinones

2-(1-Hydroxyalkyl)azetidines react with bis(trichloromethyl) carbonate (BTC) after basic treatment to afford 4-(2-chloroethyl)oxazolidinones. The scope of this rearrangement was examined in detail and its efficiency was shown to depend on the class of the