20990-17-4

Upstream product

• 20923-24-4 2,2,4-trimethyl-3-morpholin-4-yl-cyclohex-3-enone 
• 20990-14-1 2,4-dimethyl-1,3-cyclohexanedione 
• 74-88-4 methyl iodide 
• 565-69-5 ethyl isopropyl ketone 
• 1663-39-4 tert-Butyl acrylate 
• 96-22-0 pentan-3-one 
• 140-88-5 ethyl acrylate 

Downstream Products

• 163889-13-2 3-Hydrazono-2,2,6-trimethyl-cyclohexanone 
• 150966-66-8 C₂₄H₃₈N₂O₃S 

Relevant academic research and scientific papers

A convenient synthesis of 2,2,4-trimethylcyclohexane 1,3-dione: A useful precursor for the taxoid a ring

A simple and inexpensive route to the title compound is described which should be readily amenable to large scale synthesis. Thus, reaction of 3- pentanone with methyl acrylate in the presence of sodium methoxide provided 2,4-dimethylcyclohexane-1,3-dione

Total synthesis of (±)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate

Figur Presented The total synthesis of the diterpene kellermanoldione 1 is reported. Stepwise [4 + 2] cycloaddition of the ketal diene 8 and the allenoste 3 afforded the exo adduct 10x as the major product. It was converted into 1 via six steps, among them a key nonconjugative hydrolysis of a γ-methylene silyl enol ether

Revisiting [3 + 3] route to 1,3-cyclohexanedione frameworks: Hidden aspect of thermodynamically controlled enolates

We have revisited the traditional consecutive Michael-Claisen [3 + 3] process (MC-[3+3]) promising the synthesis of a cyclohexane-1,3-dione derivatives from nonactivated simple ketones and enoates and evaluated its potential in modern organic synthesis. Twenty to thirty examples were demonstrated to be effective. The reactions exhibited remarkable regioselectivity with the Michael addition proceeding through nucleophilic attack by the more hindered site of the ketones without exception. The subsequent Claisen condensation resulted in the formation of carbon-carbon bonds between less hindered site of the ketones and acyl carbon of the enoates. The MC-[3+3] process described is useful for the synthesis of Taxol A-ring synthons in multigram quantities and for the synthesis of other six-membered carbocyclic compounds. A number of control experiments have been conducted to provide strong support for the mechanism of this MC-[3+3].