1241952-10-2

Upstream product

• 1241952-09-9 C₂₃H₃₆O₃Si 
• 1241952-05-5 (S)-dec-4-yne-1,2-diol 
• 1241952-07-7 (S)-2-benzoyloxydec-4-yn-1-ol 
• 628-71-7 1-Heptyne 
• 24948-66-1 1-allyl-2-pentylacetylene 
• 98-88-4 benzoyl chloride 
• 1241952-08-8 C₁₆H₃₂O₂Si 

Downstream Products

• 1241952-11-3 (1E,3S)-3-benzoyloxy-1-iodoundec-1-en-5-yne 

Relevant academic research and scientific papers

Enantioselective synthesis of (1E, 3S)-1-iodoundec-1-en-5-yn-3-ol, the eicosanoid synthon

A synthesis of the title compound, the synthon for the constanolactones and other eicosanoids, has been developed from achiral starting compounds. The synthesis is based on the S-enantiodirected dihydroxylation of the double bond to introduce a chirality and on the use of conformational restriction of the triple bond (the latent Z-double bond) surroundings.