81757-13-3

Upstream product

• 870-63-3 prenyl bromide 
• 81757-09-7 (2R,1'R)-2-(1'-Hydroxyaethyl)-5-methyl-4-hexensaeuremethylester 
• 98-88-4 benzoyl chloride 
• 81757-11-1 (2S,1'R)-2-(1'-Hydroxyaethyl)-5-methyl-4-hexen-1-ol 

Downstream Products

• 59550-37-7 (2R)-Benzoesaeure(2-isopropenyl-5-methyl-4-hexenyl)ester 
• 498-16-8 (R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-ol 
• 81757-15-5 (2S)-Benzoesaeure(2-acetyl-5-methyl-4-hexenyl)ester 

Relevant academic research and scientific papers

C45- and C50-Carotenoids, 1st Communication. Synthesis of (R)- and (S)-Lavandulol

Starting with methyl (3R)-3-hydroxybutanoate ((R)-7) and ethyl (3S)-3-hydroxybutanoate ((S)-11), respectively, (R)- and (S)-lavandulol ((R)-1 and (S)-1) were synthesized with high optical purity.The synthesized key intermediates (R)-6 and (S)-6 are suitable compounds for the synthesis of optically active acyclic C45- and C50-carotenoids.