137449-07-1

Upstream product

• 87769-39-9 2,2,5,6-tetramethyl-2H,4H-1,3-dioxin-4-one 
• 5396-89-4 benzyl acetoacetate 
• 114473-84-6 5-Bromomethyl-2,2,6-trimethyl-[1,3]dioxin-4-one 

Relevant academic research and scientific papers

Synthesis of 1,3-dioxin-4-ones having chiral hydroxyalkyl groups at the 6-position by means of baker's yeast reduction and their uses for epc synthesis

Prochiral methyl ketones connected with 6-(4-oxo-1,3-dioxinyl) group directly or through methylene chain (1-3) gave, by treatment with fermenting baker's yeast, the corresponding (S)-alcohols which served as synthons for a variety of enantiomerically pure