19245-69-3

Usage

InChI:InChI=1/C11H20O/c1-8-5-6-9(7-10(8)12)11(2,3)4/h9-10,12H,1,5-7H2,2-4H3

Upstream product

• 100052-57-1 2-Hydroxymethylen-5-tert-butyl-cyclohexanon-81) 
• 73925-26-5 <(4-tert-Butylcyclohexyliden)methyl>-phenyl-sulfoxid 
• 936-99-2 3-tert-butylcyclohexanone 
• 98-53-3 4-tercbutyl-cyclohexanone 

Downstream Products

• 5937-40-6 trans-5-(1,1-dimethylethyl)-2-methylcyclohexanone 
• 128749-69-9 (1R,2R,4R)-4-tert-Butyl-1-hydroxymethyl-cyclohexane-1,2-diol 
• 128749-69-9 (1S,2R,4R)-4-tert-Butyl-1-hydroxymethyl-cyclohexane-1,2-diol 
• 68211-39-2 cis 4-tert-butyl-2-methoxymethylene cyclohexane 
• 73803-32-4 (-)-cis-(1S,5S)-2-methylene-5-t-butylcyclohexanol 
• 466635-89-2 (+)-cis-(1R,5R)-2-methylene-5-t-butylcyclohexanol 

Relevant academic research and scientific papers

Stereoselective Synthesis of Alcohols, I Synthesis of One-Carbon Homologous Allyl Alcohols from Aldehydes or Ketones

The high yield conversion of aldehydes and ketones 2 to the one-carbon homologous allyl alcohols 3 is achieved by condensation to the vinyl sulfoxides 7, isomerisation to the allyl sulfoxides 9, and subsequent sigmatropic rearrangement.