119092-07-8

Upstream product

• 59058-17-2 1-oxoheptan-2-yl benzoate 
• 155485-49-7 C₂₈H₃₈O₆ 
• 155555-69-4 C₃₁H₄₂O₆ 
• 155555-68-3 (6R,7R,8R,9R)-7,8-O-isopropylidene-6,7,8,9-tetradecanetetraol 
• 98-88-4 benzoyl chloride 
• 66-25-1 hexanal 
• 52513-06-1 3-(1-octen)-yl benzoate 

Downstream Products

• 121372-64-3 Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester 
• 159716-60-6 Benzoic acid (R)-1-((E)-3-oxo-propenyl)-hexyl ester 
• 119008-08-1 (-) 4-hydroxy-2-nonenal 
• 159716-65-1 Benzoic acid (R)-1-((E)-3,3-dimethoxy-propenyl)-hexyl ester 

Relevant academic research and scientific papers

A practical synthesis of (R)- and (S)-(E)-4-hydroxyalk-2-enals, cytotoxic products of the microsomal lipid peroxidation

The chemical synthesis of some (S)- and (R)-(E)-4-hydroxyalk-2-enals, important products of lipid peroxidation (LPO), has been carried out via enantiomerically pure 2-benzoyloxyaldehydes, chiral key intermediates obtained from two diastereomeric diepoxide

RESOLUTION AND DETERMINATION OF ENANTIOMERIC EXCESSES OF CHIRAL ALDEHYDES VIA CHIRAL IMIDAZOLIDINES

Enantiomeric purity of chiral aldehydes was determined by NMR analysis of derived imidazolidines.The diastereomeric imidazolidines were easily separated by silica gel column and converted into enantiomerically pure aldehyde by acid hydrolysis.