1338645-91-2

Upstream product

• 1338645-50-3 N-[(1S)-1-(1-naphthyl)ethyl]-5-hexynamide 
• 1338645-58-1 benzyl N-(5-hexynoyl)-N-[(1S)-1-(1-naphthyl)ethyl]carbamate 
• 1338645-66-1 benzyl N-[(1S)-1-(1-naphthyl)ethyl]-N-{1-[(trimethylsilyl)oxy]-5-hexynyl}carbamate 
• 1338645-87-6 C₄₄H₄₄N₂O₅ 
• 1338645-88-7 C₄₃H₄₄N₂O₇ 
• 1338645-89-8 C₅₉H₅₉N₃O₈ 
• 1338645-90-1 C₄₇H₄₉N₃O₈ 
• 55183-45-4 hex-5-in-carboxyl chloride 

Relevant academic research and scientific papers

Expedient synthesis of chiral homoallylamines via N, O-acetal TMS ethers and its application

A highly stereoselective and efficient method for the synthesis of optically active homoallylamines was developed. Key features of the method include (1) the utilization of naphthylethylamine as both an excellent chiral auxiliary and the amine source, (2)