119435-10-8

Upstream product

• 119385-30-7 (3S,5R)-3-Butyl-5-trimethylsilanyl-cyclohexanone 
• 1694-31-1 tert-butyl acetoacetate 
• 18829-55-5 (E)-2-Heptenal 
• 244109-51-1 C₁₈H₂₈OSi 
• 119390-02-2 (3R,5R)-3-Butyl-5-trimethylsilanyl-1-trimethylsilanyloxy-cyclohexene 
• 116215-94-2 (R)-(-)-5-trimethylsilyl-2-cyclohexenone 

Downstream Products

• 119435-11-9 ((R)-3-Butyl-cyclohexa-1,5-dienyloxy)-trimethyl-silane 

Relevant academic research and scientific papers

A simple asymmetric organocatalytic approach to optically active cyclohexenones

Optically active 2,5-disubstituted-cyclohexen-2-one derivatives have been prepared in a one-pot process consisting of five reaction steps: an organocatalytic asymmetric conjugated addition of β-ketoesters to α,β-unsaturated aldehydes that proceeds in aque

Simple and practical routes to enantiomerically pure 5-(Trialkylsilyl)-2-cyclohexenones

Formula presented Enantiomerically pure chiral 5-silylated 2-cyclohexenones are easily prepared in high yield using as a key step kinetic resolution with a commercially available lipase. Fully active enzyme can be recovered very efficiently for reuse. The

Synthesis of (R)-(+)-4-Butyl-2,6-cycloheptadienone, a Constituent of Marine Algae

The title compound was synthesized from (R)-(-)-5-trimethylsilyl-2-cyclohexenone in 19percent overall yield.