132604-14-9

Upstream product

• 132604-12-7 5-[(S)-3-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-butylidene]-2,2-dimethyl-[1,3]dioxane-4,6-dione 
• 132604-10-5 5-((3S)-1,3-dihydroxybutylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione 
• 132604-13-8 (S)-5-(tert-Butyl-diphenyl-silanyloxy)-3-oxo-hexanoic acid methyl ester 
• 74-88-4 methyl iodide 
• 84257-12-5 2,2-dimethyl-5-(1-hydroxy-3-oxobutylidene)-1,3-dioxane-4,6-dione 

Relevant academic research and scientific papers

Highly enantioselective reduction of acetoacetylated Meldrum's acid with fermenting baker's yeast

Acetoacetylated Meldrum's acid was enantioselectively reduced with fermenting baker's yeast to afford the corresponding chiral (S)-alcohol, which could be easily converted to δ-lactone derivatives.