871809-99-3

Upstream product

• 871809-97-1 (4S,6R)-4-[(R)-2-benzyloxy-4-(4-benzyloxyphenyl)butyl]-2,2-dimethyl-6-n-tridecyl-[1,3]dioxane 
• 871809-93-7 (+)-(3R)-1-[4-(benzyloxy)phenyl]hex-5-en-3-ol 
• 871809-94-8 (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hex-1-ene 
• 871809-95-9 (R)-4-benzyloxy-6-(4-benzyloxyphenyl)hexan-2-one 
• 871809-96-0 (3R,5R,7R)-3-benzyloxy-1-(4-benzyloxyphenyl)eicosane-5,7-diol 
• 68486-77-1 3-(4-(benzyloxy)phenyl)propanal 

Downstream Products

• 913814-39-8 1-[(4R,6R)-(2,2-dimethyl-6-tridecyl-[1,3]dioxan-4-yl)]-4-(4-hydroxyphenyl)-butan-2-one 

Relevant academic research and scientific papers

Enantioselective synthesis and absolute configurations of aculeatins A, B, D, and 6-epi-aculeatin D

The three naturally occurring, bioactive spiroacetals aculeatins A, B, and D, as well as the non-natural 6-epi-aculeatin D have been synthesized for the first time in enantiopure form using an asymmetric allylation as the only chirality source. A further

Enantioselective synthesis and absolute configurations of aculeatins A and B

The two naturally occuring, bioactive spiroacetals aculeatins A and B have been synthesized for the first time in enantiopure form using an asymmetric allylation as the only chirality source. A further key step was a stereoselective aldol reaction with re