22472-77-1

Upstream product

• 2623-23-6 L-menthyl acetate 
• 619-52-3 (1R)-menth-3-ene 
• 53798-07-5 (1R,5S)-1-isopropyl-5-methylcyclohex-2-enol 
• 29685-68-5 (1R,4R,6R)-1-isopropyl-4-methyl-7-oxa-bicyclo[4.1.0]heptan-2-one 
• 555-31-7 aluminum isopropoxide 
• 53798-08-6 (S)-(+)-p-menth-4-en-3-one 
• 1753-40-8 (R)-4-menthen-3-one 

Downstream Products

• 1678-82-6 trans-1,4-menthane 
• 23283-97-8 (+)-(1S,2R,5R)-isomenthol 
• 1753-40-8 (R)-4-menthen-3-one 

Relevant academic research and scientific papers

Reactions of (R)-4-Menthen-3-one with Aluminum and Boron-Containing Hydrides

It was shown that the most effective and stereospecific hydride reductant for (R)-4-menthen-3-one to (1R,3R)-menthen-3-ol was i-Bu2AlH whereas the complex BH3·THF, which exhibited the same properties relative to the substrate carbony

Synthetic studies of didemnaketal analogue - Construction of the (+)- and (-)-5,6-dihydroxy-3,7-dimethyl-octanal intermediates

A synthetic procedure for construction of the (+)-(3R,5R,6R)-5,6- dihydroxy-3,7-dimethyl-octanal and (-)(3S,5S,6S)-5,6-dihydroxy-3,7-dimethyl- octanal derivatives, the intermediates for synthesis of the HIV-active di- demnaketal analogue, was developed via a series of reactions from the natural (-)-menthone.