181955-91-9

Upstream product

• 22081-10-3 2-(4-Hydroxybenzyl)-1-cyclohexanone 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 150821-14-0 trans-(1R,2S)-2-(4-hydroxybenzyl)-1-cyclohexanol 
• 150821-13-9 trans-(1S,2R)-2-(4-hydroxybenzyl)-1-cyclohexanol 
• 150821-12-8 (1R,2R)-cis-2-(4-hydroxybenzyl)-1-cyclohexanol 
• 218462-38-5 3-[(S)-1-(4-Methoxymethoxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 218462-41-0 3-[(R)-1-(4-Methoxymethoxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 218462-53-4 3-[1-(4-Methoxymethoxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 218462-43-2 3-[(S)-1-(4-Hydroxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 218462-44-3 3-[(R)-1-(4-Hydroxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 218462-45-4 3-[1-(4-Hydroxy-benzyl)-2-oxo-cyclohexyl]-propionic acid methyl ester 
• 158703-34-5 trans-(1S,2R)-2-(4-methoxymethoxybenzyl)-1-cyclohexanol 
• 158703-32-3 cis-(1S,2S)-2-(4-methoxymethoxybenzyl)-1-cyclohexanol 

Relevant academic research and scientific papers

Chiral juvenoids derived from 2-substituted cyclohexanols

Chiral juvenoids 1d-4d were prepared by a chemoenzymatic process consisting in employing microorganism-mediated biotransformations and/or enzyme-mediated transformation of convenient substrates, followed by a chemical transformation of the chiral intermed