905588-48-9

Upstream product

• 197074-41-2 (R,E)-4-hydroxy-6-phenylhex-5-en-2-one 
• 905588-51-4 (E)-(R)-5-Methyl-1-phenyl-octa-1,7-diene-3,5-diol 
• 905588-03-6 (R,E)-5-oxo-1-phenylhex-1-en-3-yl acetate 

Relevant academic research and scientific papers

Enzymatic approach to enantiomerically pure 5-alken-2,4-diols and 4-hydroxy-5-alken-2-ones: Application to the synthesis of chiral synthons

Enantiomerically pure 1,3-diols 1-3 were obtained by a chemoenzymatic approach (lipase PS from Burkholderia cepacia). These diols were converted into useful chiral synthons, which could be considered homologues of glyceraldehyde and glyceric acid acetonid