137449-14-0

Upstream product

• 130473-34-6 (S)-6-(1-Hydroxyethyl)-2,2-dimethyl-1,3-dioxin-4-one 
• 130473-32-4 6-Acetyl-2,2-dimethyl-1,3-dioxin-4-one 
• 128766-64-3 6-(1-Hydroxyethyl)-2,2-dimethyl-1,3-dioxin-4-one 
• 130473-35-7 (S)-6-(1-tert-Butyldimethylsilyloxyethyl)-2,2-dimethyl-1,3-dioxin-4-one 
• 538-75-0 dicyclohexyl-carbodiimide 

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