871820-99-4

Upstream product

• 102308-32-7 (4S)-4-formyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester 
• 108149-63-9 4-hydroxymethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 1377320-83-6 (S)-tert-butyl 4-(hydroxy(phenyl)methyl)-2,2-dimethyloxazolidine-3-carboxylate 

Downstream Products

• 871821-01-1 ((1R,2R)-1-Furan-2-yl-2-methoxymethoxy-2-phenyl-ethyl)-carbamic acid tert-butyl ester 
• 871821-49-7 (2S,3S,4S,5S)-3,4,5-Trihydroxy-2-((R)-methoxymethoxy-phenyl-methyl)-piperidine-1-carboxylic acid tert-butyl ester 
• 871821-43-1 6-ethoxy-3-hydroxy-2-(methoxymethoxy-phenyl-methyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 871821-40-8 6-ethoxy-2-(methoxymethoxy-phenyl-methyl)-3-oxo-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 871821-37-3 6-hydroxy-2-(methoxymethoxy-phenyl-methyl)-3-oxo-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 871821-46-4 3-hydroxy-2-(methoxymethoxy-phenyl-methyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 

Relevant academic research and scientific papers

Preparation of enantiomerically pure 2-(1′-aminomethyl)furan derivatives and synthesis of an unnatural polyhydroxylated piperidine

Zinc-mediated propargylation of α-acylaminoaldehydes, and subsequent oxidative isomerization followed by Ag(I)-catalyzed cycloisomerization conveniently provides a new enantioselective route to the corresponding 2-aminoalkylfurans. One of these furans was