270925-36-5

Upstream product

• 270925-35-4 dimethyl (4S)-4-[N-((1R)-1-phenylethyl)-2,2,2-trifluoroacetylamino]-2-methylenepentane-1,5-dioate 

Downstream Products

• 553679-35-9 methyl 2-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}-3-(5-{(1R,2R)-1-triethylsilyloxy-3-[(4-methylphenyl)sulfonyloxy]-2-phenylcarbonyloxypropyl}(2R,4R)-4-hydroxy-2-(methoxycarbonyl)oxolan-2-yl)(2S)propanoate 
• 553679-34-8 methyl 3-((2R)-5-{(1R,2R)-1-triethylsilyloxy-3-[(4-methylphenyl)sulfonyloxy]-2-phenylcarbonyloxypropyl}-2-(methoxycarbonyl)-4-oxo(2-2,3,5-trihydrofuryl))-2-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}(2S)propanoate 
• 553679-33-7 methyl 2-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}-3-(5-{(1R,2R)-1-triethylsilyloxy-3-[(4-methylphenyl)sulfonyloxy]-2-phenylcarbonyloxypropyl}(2S)-2-(methoxycarbonyl)-4-methylene(2-2,3,5-trihydrofuryl))(2S)propanoate 
• 553679-29-1 methyl 2-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}-3-(5-{(1R,2R)-1-hydroxy-3-[(4-methylphenyl)sulfonyloxy]-2-phenylcarbonyloxypropyl}(2S)-2-(methoxycarbonyl)-4-methylene(2-2,3,5-trihydrofuryl))(2S)propanoate 
• 553679-31-5 methyl 3-((2R)-5-{(1R,2R)-1-hydroxy-3-[(4-methylphenyl)sulfonyloxy]-2-phenylcarbonyloxypropyl}-2-(methoxycarbonyl)-4-oxo(2-2,3,5-trihydrofuryl))-2-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}(2S)propanoate 
• 553679-28-0 dimethyl 2-[2-(3-{(1R)-2-[(4-methylphenyl)sulfonyloxy]-1-phenylcarbonyloxyethyl}(2R,3R)oxiran-2-yl)prop-2-enyl]-4-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}(2S,4S)-2-hydroxypentane-1,5-dioate 
• 553679-27-9 dimethyl 2-[2-(3-{(1R)-1-hydroxy-2-[(4-methylphenyl)sulfonyloxy]ethyl}(2R,3R)oxiran-2-yl)prop-2-enyl]-4-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}(2S,4S)-2-hydroxypentane-1,5-dioate 
• 553679-26-8 dimethyl 4-{N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino}-2-{(5S)(3Z)-5-hydroxy-2-methylene-6-[(4-methylphenyl)sulfonyloxy]hex-3-enyl}(2S,4S)-2-hydroxypentane-1,5-dioate 
• 553679-25-7 dimethyl 4-[N-[(1R)-1-phenylethyl]-2,2,2-trifluoroacetylamino]-2-[(5S)(3Z)-5,6-dihydroxy-2-methylenehex-3-enyl](2S,4S)-2-hydroxypentane-1,5-dioate 

Relevant academic research and scientific papers

Aldol reaction under solvent-free conditions: Highly stereoselective synthesis of 1,3-amino alcohols

(formula presented) A method for the highly stereoselective synthesis of 1,3-amino alcohols based on the indium trichloride-catalyzed Mukaiyama aldol reaction of keto ester (R,S)-1 under solvent-free conditions has been developed. The high selectivity obs