1233719-75-9

Upstream product

• 183508-07-8 (R,E)-1-(tert-butyldiphenylsilyloxy)pent-3-en-2-ol 
• 853916-88-8 (-)-(E)-(R)-2-hydroxypent-3-enoic acid ethyl ester 
• 1233719-69-1 (2S,4S)-2,4,6-trimethylheptan-1-ol 
• 176900-61-1 (2S,4R)-2,4-dimethyl-5-(tosyloxy)pentyl acetate 
• 90270-02-3 (2R,4S)-1-hydroxy-2,4-dimethylpentyl acetate 
• 2121-69-9 (2R,4S)-2,4-dimethylpentane-1,5-diol 
• 4295-92-5 (3R,5S)-3,5-dimethyldihydro-2H-pyran-2,6(3H)-dione 
• 143289-04-7 trans-(2R)-1,2-dihydroxy-3-pentene 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 1184621-40-6 2-diphenylphosphanyl-benzoic acid (E)-(R)-1-(tert-butyl-diphenyl-silanyl-oxymethyl)-but-2-enyl ester 
• 1233719-74-8 (2S,4S)-1-bromo-2,4,6-trimethylheptane 

Relevant academic research and scientific papers

METHOD FOR PREPARING VITTATALACTONE

The present invention relates to the chemical synthesis of vittatalactone, the aggregation pheromone of the striped cucumber beetle, Acalymma vittatum.

Enantioselective total synthesis of the unnatural and the natural stereoisomers of vittatalactone

(Figure presented) The striped cucumber beetle, Acalymma vittatum, is a cause of major damage to cucurbit crops in North America. To develop an environmentally benign plant protection strategy, recent research has focused on identifying sex pheromones of