1192344-65-2

Upstream product

• 1174752-28-3 2-diphenylphosphanyl-benzoic acid (E)-(S)-1-(tert-butyl-diphenyl-silanyl-oxymethyl)-but-2-enyl ester 
• 1192344-62-9 (2R,4R)-1-bromo-2,4,6-trimethylheptane 
• 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 
• 1192344-67-4 (2R,4R)-2,4,6-trimethylheptan-1-ol 
• 1192344-64-1 (5R,7R,E)-5,7,9-trimethyldec-3-ene 
• 1059044-36-8 (-)-(2S)-trifluoromethanesulfonyloxy-4-methyl-pentanoic acid tert-butyl ester 
• 1233719-68-0 (R)-1-bromo-2,4-dimethylpentane 
• 1192344-63-0 (R)-1-((2,4-dimethylpentyloxy)methyl)-4-methoxybenzene 
• 1184621-40-6 2-diphenylphosphanyl-benzoic acid (E)-(R)-1-(tert-butyl-diphenyl-silanyl-oxymethyl)-but-2-enyl ester 
• 125427-94-3 (-)-(2R,4)-dimethyl-pentanoic acid tert-butyl ester 
• 1233719-72-6 (R,E)-5,7-dimethyloct-3-ene 
• 143289-04-7 trans-(2R)-1,2-dihydroxy-3-pentene 
• 58479-61-1 tert-butylchlorodiphenylsilane 

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

Enantioselective total synthesis and determination of absolute configuration of vittatalactone

The first asymmetric total synthesis of vittatalactone features the divergent synthesis of two dlastereomers to assign the absolute configuration of the natural product. Its consecutive propionate and deoxyproponate stereogenic centers are established by