160452-48-2

Upstream product

• 160452-46-0 methyl 3-heptanoyl-2,3,4,5-tetrahydro-2-thioxo-1,3-oxazole-4-carboxylate 
• 137306-81-1 methyl (R)-3-<(tert-butyl)dimethylsilyloxy>tetradecanoate 
• 137306-82-2 (R)-3-<(tert-butyl)dimethylsilyloxy>tetradecanal 
• 111-64-8 n-octanoic acid chloride 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 76062-97-0 methyl (R)-3-hydroxytetradecanoate 
• 2462-31-9 benzyl 2-aminoacetate hydrochloride 
• 160452-47-1 methyl (R)-3-<(2S,3R,5R)-5-<(tert-butyl)dimethylsilyloxy>-2-hexyl-3-hydroxyhexadecanoyl>-2,3,4,5-tetrahydro-2-thioxooxazole-4-carboxylate 

Downstream Products

• 160452-43-7 benzyl (2S,3S)-2-<(R)-2-<(tert-butyl)dimethylsilyloxy>tridecyl>-3-hexyl-4-oxoazetidine-1-acetate 
• 160452-49-3 benzyl (2S,3S)-3-hexyl-2-<(R)-2-hydroxytridecyl>-4-oxoazetidine-1-acetate 
• 1026915-39-8 [(2S,3R,5R)-5-(tert-Butyl-dimethyl-silanyloxy)-2-hexyl-3-methanesulfonyloxy-hexadecanoylamino]-acetic acid benzyl ester 

Relevant academic research and scientific papers

Stereoselective syntheses of tetrahydroesterastin-β-lactam analogues

A total synthesis of the optically active tetrahydroesterastin-β-lactam analogue 2 using Miller's hydroxamate approach is described (Scheme 2). Significant modification of published procedures has resulted in a short and facile stereospecific preparation