180406-85-3

Upstream product

• 65844-86-2 5-(benzyloxy)pent-3-yn-2-one 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Downstream Products

• 180406-86-4 2-(5-benzyloxy-2-oxo-3-pentynyl)-1-(t-butoxycarbonyl)pyrrolidine 
• 794528-61-3 stemoamide 
• 180407-00-5 2-(2-Benzoyloxy-5-methanesulfonyloxy-pentyl)-5-oxo-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 180406-99-9 2-(2-Benzoyloxy-5-methanesulfonyloxy-pentyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 180407-05-0 2-(5-Benzyloxy-1-tert-butoxycarbonylmethyl-2-oxo-pent-3-ynyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 180406-97-7 2-(2-Benzoyloxy-5-benzyloxy-pentyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 180406-98-8 2-(2-benzoyloxy-5-hydroxypentyl)-1-(t-butoxycarbonyl)pyrrolidine 
• 180407-01-6 Benzoic acid 4-methanesulfonyloxy-1-(5-oxo-pyrrolidin-2-ylmethyl)-butyl ester 
• 180406-95-5 2-(5-benzyloxy-2-oxopentyl)-1-(t-butoxycarbonyl)pyrrolidine 
• 180406-96-6 2-(5-Benzyloxy-2-hydroxy-pentyl)-pyrrolidine-1-carboxylic acid tert-butyl ester 
• 180407-03-8 7-Benzyloxy-4-oxo-hept-5-ynoic acid tert-butyl ester 

Relevant academic research and scientific papers

Synthesis of (±)-stemonamide by the application of oxidative coupling reactions of stannyl compounds with silyl enol ethers

A tricyclic Stemona alkaloid, (±)-stemonamide, can be synthesized by applying the oxidative coupling reactions of stannyl compounds with silyl enol ethers to construct the carbon skeleton.