113793-68-3

Upstream product

• 109-72-8 n-butyllithium 
• 113793-67-2 phenyl β-cyclothiogeranate 
• 79-37-8 oxalyl dichloride 
• 58254-14-1 2,6,6-trimethylcyclohexene-1-carbonyl chloride 
• 108-98-5 thiophenol 

Relevant academic research and scientific papers

Process for the preparation of cycloaliphatic ketones

Process for the preparation of cycloaliphatic ketones of formula STR1 wherein index m designates integer 0, 1 or 2, n stands for 0 or 1 and the dotted lines represent an optional supplemental bond, which process consists in the deprotonation of an ester o

Reaction of Ester Enolates with Nucleophiles. Stereocontrolled Formation of Ketone and Aldehyde Enolates

Lithium enolates of carboxylic and thiocarboxylic esters react with nucleophiles to afford ketone and aldehyde enolates and subsequently their enol silyl ethers diastereoselectively.This reaction is applied to the synthesis of γ-damascone, α-damascone, β-safranal, and artemisia ketone.