108149-91-3

Upstream product

• 108149-88-8 (2R,3R)-1,2-O-isopropylidene-4-(N-benzylcarbamyl)-3-chlorobutane-1,2,4-triol 
• 108149-89-9 (4S,1'S)-3-benzyl-4-<1,2-(isopropylidenedioxy)ethyl>-1,3-oxazolidin-2-one 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 108149-90-2 (4S,1'S)-3-benzyl-4-(1,2-dihydroxyethyl)-1,3-oxazolidin-2-one 

Downstream Products

• 108149-92-4 (4S,1'S)-3-benzyl-4-<1-(benzyloxy)-2-((tert-buthyldimethylsilyl)oxy)ethyl>-1,3-oxazolidyn-2-one 
• 108149-95-7 (4S,1'S)-3-benzyl-4-<2-acethoxy-1-(benzyloxy)-3-(phenylsulfonyl)hexadecyl>-1,3-oxazolidyn-2-one 
• 108149-96-8 (2'E,4S,1'R)-3-benzyl-4-<1-(benzyloxy)hexadec-2-enyl>-1,3-oxazolidyn-2-one 
• 108149-94-6 (4S,1'S)-3-benzyl-4-<1-(benzyloxy)-2-oxoethyl>-1,3-oxazolidyn-2-one 
• 108149-93-5 (1S,1'S)-3-benzyl-4-<1-(benzyloxy)-2-hydroxyethyl>-1,3-oxazolidyn-2-one 

Relevant academic research and scientific papers

Fumarase-Catalyzed Synthesis of L-threo-Chloromalic Acid and Its Conversion to 2-Deoxy-D-ribose and D-erythro-Sphingosine

This paper describes the use of pig heart fumarase (E.C. 4.2.1.2) as a catalyst in the multigram synthesis of L-threo-chloromalic acid (1) (>99.5percent enantiomeric excess) on 50-g scale.L-threo-Fluoromalic acid has been synthesized in a coupled enzymic system from difluorofumaric acid.Compound 1 serves as starting material for syntheses of 2-deoxy-D-ribose and D-erythro-sphingosine.