150698-29-6

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 150960-19-3 (2S,3S)-1,2,3-trihydroxytetradecane 
• 51309-22-9 tetradec-2-yn-1-ol 
• 693-67-4 bromoundecane 
• 105678-96-4 [(2S,3R)-3-undecyloxiran-2-yl]methanol 
• 75039-85-9 cis-tetradec-2-ene-1-ol 
• 150698-27-4 [(4S,5S)-2,2-Dimethyl-5-((E)-undec-1-enyl)-[1,3]dioxolan-4-yl]-methanol 
• 150822-77-8 (2S,3S)-2,3-O-Isopropylidene-1,2,3-tetradecanetriol 

Downstream Products

• 150822-79-0 (2S,3S)-1,2-epoxy-3-(tosyloxy)tetradecane 

Relevant academic research and scientific papers

Method for synthesizing (3Z,6Z,9S,10R)-9,10-epoxy-3,6-heneicosadiene

The invention belongs to the technical field of green pesticides, and discloses a novel method for synthesizing a main active component (3Z,6Z,9S,10R)-9,10-epoxy-3,6-heneicosadiene of sex pheromone of fall webworms. The method comprises the steps: by taki

Access to unsaturated chiral epoxides. Part II. Synthesis of a component of the sex pheromone of Phragmatobia fuliginosa

A general method for the synthesis of chiral cis-epoxides substituted bearing a saturated chain and an unsaturated chain is described. This method is used to synthesize both enantiomers of compound 1.

Alkylative Epoxide Rearrangement. A Stereospecific Approach to Chiral Epoxide Pheromones

The alkylative rearrangement of 1,2-epoxy-3-alkanol tosylates is applied to the synthesis of chiral epoxide pheromones.Attack at the terminal carbon atom of epoxy tosylates by lithioacetylenes and cyclization of the intermediate tosyloxy alcohols produces