151698-79-2

Upstream product

• 75-24-1 trimethylaluminum 
• 131484-41-8 erythro-(2R,3S)-4-(tert-butyldimethylsiloxy)-2,3-epoxy-1-butanol 
• 917-54-4 methyllithium 

Downstream Products

• 155073-31-7 (4S,5S)-4-Methyl-5-nonanol 
• 155073-35-1 (2R,3S,2'RS)-1-tert-butyldiphenylsilyloxy-3-methyl-2-(tetrahydro-2'H-pyran-2'-yloxy)hexane 
• 163381-99-5 (2R,3S,2'RS)-3-methyl-2-(tetrahydro-2'H-pyran-2'-yloxy)hexyl p-toluenesulfonate 
• 163381-98-4 (2R,3S,2'RS)-3-methyl-2-(tetrahydro-2'H-pyran-2'-yloxy)-1-hexanol 
• 163381-97-3 (2S,3R,2'RS)-4-tert-butyldiphenylsilyloxy-2-methyl-3-(tetrahydro-2'H-pyran-2'-yloxy)butyl p-toluenesulfonate 
• 173852-53-4 (2R,3S)-1-(tert-Butyldiphenylsilyloxy)-3-methyl-4-(pivaloyloxy)-2-butanol 
• 154955-38-1 (2S,3R)-4-tert-butyldiphenylsilyloxy-2-methyl-3-hydroxylbutyl p-toluenesulfonate 

Relevant academic research and scientific papers

Pheromone Synthesis, CLXXI. A New Synthesis of (2E,4E,6R,10R)-4,6,10,12-Tetramethyl-2,4-tridecadien-7-one (Matsuone), the Primary Component of the Sex Pheromone of Three Matsucoccus Pine Bast Scales

A new synthesis of (2E,4E,6R,10R)-4,6,10,12-tetramethyl-2,4-tridecadien-7-one (1; matsuone) was achieved by starting from (2R,3S)-4-(tert-butyldiphenylsilyloxy)-2,3-epoxy-1-butanol (21 = E) and methyl (R)-3-hydroxy-2-methylpropanoate (2 = I).Cleavage of 2

Pheromone Synthesis, CLIV. Synthesis of the Stereoisomers of 3-Methyl-4-octanol to Determine the Absolute Configuration of the Naturally Occuring (3S,4S)-Isomer Isolated as the Male-Produced Aggregation Pheromone of the African Palm Weevil, Rhynchophorus

The relative configuration of the naturally occuring 3-methyl-4-octanol (1), the male-produced aggregation pheromone of Rhynchophorus phoenicis, was determined as syn by a GC comparison of the synthetic (+/-)-syn- and (+/-)-anti-1 with the natural product