133475-85-1

Upstream product

• 133475-75-9 Toluene-4-sulfonic acid (2S,3S)-2,3-dihydroxy-8-methyl-nonyl ester 
• 141034-27-7 (4R,5S)-2,2-Dimethyl-5-(5-methyl-hexyl)-[1,3]dioxolane-4-carbaldehyde 
• 141034-27-7 (4S,5S)-2,2-Dimethyl-5-(5-methyl-hexyl)-[1,3]dioxolane-4-carbaldehyde 
• 133575-34-5 [(4S,5S)-2,2-Dimethyl-5-(5-methyl-hexyl)-[1,3]dioxolan-4-yl]-methanol 
• 133475-64-6 [(4R,5S)-2,2-Dimethyl-5-(5-methyl-hexyl)-[1,3]dioxolan-4-yl]-methanol 
• 133475-80-6 (S)-6-Methyl-1-(S)-oxiranyl-heptan-1-ol 
• 39110-24-2 (3-Methyl-butylidene)-triphenyl-λ⁵-phosphane 
• 86795-44-0 3,4-O-isopropylidene-2-deoxy-D-ribose 
• 39691-62-8 nonylmagnesium bromide 

Downstream Products

• 54848-41-8 *,R^*)>-2-Methyl-7,8-octadecandiol,7-(4-methyl-benzolsulfonat) 

Relevant academic research and scientific papers

Synthesis of chiral epoxy alcohols: Synthesis of (+)-disparlure

(2R,3S)-1,2-Epoxy alcohols 1, (2S,3S)-2,3-epoxy alcohols 2, and (2S,3S)-1,2-epoxy alcohols 3 were prepared from readily available (-)-2-deoxy-D-ribose. Using epoxy alcohol 3b as a chiral synthon, (+)-disparlure, the pheromone of the gypsy moth, Porthetria