138877-07-3

Upstream product

• 1360170-47-3 (4S,5S)-4-ethyl-5-methyl-2-phenyl-1,3-dioxane 
• 138832-87-8 3R-methyl-4-(2R/S-tetrahydropyranyloxy)-1,2R/S-epoxybutane 
• 138832-88-9 4R-methyl-5-(2R/S-tetrahydropyranyloxy)-3R/S-pentanol 
• 129172-72-1 (R)-4-(2-tetrahydropyranyloxy)-3-methylbutene 
• 100-39-0 benzyl bromide 
• 138832-89-0 4R-methyl-5-(2R/S-tetrahydropyranyloxy)-3R/S-pentanol benzyl ether 
• 84736-38-9 (E/Z)-1-(benzyloxy)-1-(prop-1-enyloxy)propane 

Downstream Products

• 149-31-5 2-methyl-1,3-pentanediol 
• 1360170-07-5 (2R,4S,5S)-5-(benzyloxy)-2,4-dimethylheptan-1-ol 
• 84736-41-4 [S-(R*,R*)]-2-methyl-3-(phenylmethoxy)pentanal 
• 1360170-11-1 (2R,3S,4S,5S)-1-((S)-4-benzyl-2-thioxothiazolidin-3-yl)-5-(benzyloxy)-3-hydroxy-2,4-dimethylheptan-1-one 
• 1360170-52-0 (2S,3R,4S,5S)-5-(benzyloxy)-2,4-dimethylheptane-1,3-diol 
• 1360170-55-3 (2S,3R,4S,5S)-5-(benzyloxy)-1-(tert-butyldimethylsilyloxy)-2,4-dimethylheptan-3-ol 
• 1360170-58-6 O-(2S,3R,4R,5S)-5-(benzyloxy)-1-(tert-butyldimethylsilyloxy)-2,4-dimethylheptan-3-yl S-methylcarbonodithioate 
• 1360170-62-2 ((2R,4S,5S)-5-(benzyloxy)-2,4-dimethylheptyloxy)(tert-butyl)dimethylsilane 
• 1360170-65-5 (4R,6S,7S)-7-(benzyloxy)-4,6-dimethylnonan-3-one 
• 1360170-67-7 (3R,5S,6S)-6-(benzyloxy)-3,5-dimethyloctan-2-one 
• 1360170-70-2 C₁₈H₃₀O₂ 
• 72522-40-8 (4R,6S,7S)-7-hydroxy-4,6-dimethyl-3-nonanone 
• 72485-37-1 (4R,6S,7S)-7-acetoxy-4,6-dimethyl-3-nonanone 
• 138832-86-7 3R/S-benzyloxy-2R-methylpentanoic acid 3-pentyl ester 

Relevant academic research and scientific papers

Synthesis of (4R,6S,7R)-7-hydroxy-4,6-dimethyl-3-nonanone and (3R,5S,6R)-6-hydroxy-3,5-dimethyl-2-octanone

The synthesis of (4R,6S,7R)-7-hydroxy-4,6-dimethyl-3-nonanone and (3R,5S,6R)-6-hydroxy-3,5-dimethyl-2-octanone is described as their acetates using a desymmetrization strategy as well as an Evans syn aldol strategy.

SYNTHESIS OF ALL FOUR POSSIBLE ENANTIOMERS OF SITOPHILATE AGGREGATION PHEROMONE OF THE GRANARY WEEVIL

An efficient synthesis of the 3-pentyl ester of 2S-methyl-3R-hydroxypentanoic acid (sitophilate) and its 2S,3S-, 2R,3R-, and 2R,3S-isomers has been carried out starting from the available 2R-methyl-3-butenyl acetate as sole monochiral precursor.

Triisobutylaluminum-Assisted Reductive Rearrangement of Alkyl 1-Alkenyl Acetals: An Easy Synthesis of β-Alkoxy Alcohols

Alkyl 1-alkenyl acetals react with Al-i-Bu3 to give very good yields of β-alkoxy alcohols through a reductive rearrangement.The reaction is totally regioselective, but no stereocontrol occurs.