17179-64-5

Upstream product

• 201230-82-2 carbon monoxide 
• 61699-43-2 methyl 1,1-pentamethyleneprop-2-ynyl carbonate 
• 1360733-29-4 methyl (1-(3-oxoprop-1-yn-1-yl)cyclohexyl)carbonate 
• 1360733-85-2 C₁₁H₁₆O₄ 
• 1360733-83-0 1-(3-((t-butyldimethylsilyl)oxy)prop-1-yn-1-yl)cyclohexyl methyl carbonate 
• 108-94-1 cyclohexanone 
• 67-56-1 methanol 
• 78-27-3 1-Ethynylcyclohexan-1-ol 

Downstream Products

• 54526-84-0 (E)-3-(cyclohex-1-ene)-prop-2-enoic acid methyl ester 

Relevant academic research and scientific papers

Stereoselective synthesis of (Z)-α-(alkoxycarbonyl)methylene β- and γ-lactones by palladium-catalysed oxidative carbonylation of alkynols

(Z)-α-(Alkoxycarbonyl)methylene β- and γ-lactones can be obtained in fair to excellent yields and with high catalytic efficiencies by PdI2/KI-catalysed oxidative dialkoxycarbonylation of propynyl alcohols (α,α-dialkyl substituted, or α-monoalky

α-fluoroallenoate synthesis via N-heterocyclic carbene-catalyzed fluorination reaction of alkynals

The first catalytic α-fluoroallenoate synthesis is described. With a suitable combination of N-heterocyclic carbene precatalyst, base, and fluorine reagent, the reaction proceeded smoothly to yield a wide range of α-fluoroallenoates with excellent chemose

N -heterocyclic carbene-catalyzed internal redox reaction of alkynals: An efficient synthesis of allenoates

An efficient N-heterocyclic carbene (NHC)-catalyzed internal redox reaction of alkynals that bear a γ leaving group has been developed. This process provides a new access to a range of allenoates in good yields. Preliminary results demonstrate that the en

PALLADIUM-CATALYZED CARBONYLATION OF PROPARGYLIC CARBONATES: PREPARATION OF 2,3- AND 2,4-DIENYL CARBOXYLATES

Propargylic carbonates are converted to 2,3-dienyl carboxylates by the palladium-catalyzed decarboxylation-carbonylation in alcohol under mild conditions.In ether, 2,4-dienyl carboxylates are obtained.