29179-20-2

Upstream product

• 1193-18-6 3-methylcyclohexen-2-one 
• 100-52-7 benzaldehyde 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 101773-30-2 3-<(trimethylsilyl)methyl>cyclo-2-hexenone 
• 1119-40-0 Dimethyl glutarate 
• 756-79-6 dimethyl methane phosphonate 
• 5682-75-7 3-chloro-2-cyclohexenone 
• 536-74-3 phenylacetylene 
• 108162-13-6 Z-styryl n-butyltelluride 
• 88841-83-2 3-(Phenylseleno)-2-cyclohexen-1-one 
• 100-42-5 styrene 
• 77708-66-8 3-oxocyclohex-1-en-1-yl 4-methylbenzenesulfonate 
• 588-72-7 [(E)-2-bromoethenyl]benzene 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 

Downstream Products

• 29179-21-3 cis-3-styryl-2-cyclohexenone 
• 36480-47-4 3-(trans-β-Styryl)-2-cyclohexenol 
• 35840-69-8 3,5-Dinitro-benzoic acid 3-((E)-styryl)-cyclohex-2-enyl ester 
• 1354729-34-2 C₂₁H₂₂O 
• 1402434-84-7 (S,E)-3-ethyl-3-styrylcyclohexanone 
• 1630982-22-7 (E)-1-(chloromethyl)-3-styrylcyclohex-2-en-1-ol 
• 532-27-4 1-chloroacetophenone 
• 1609386-21-1 3,3-di((E)-styryl)cyclohexan-1-one 
• 1609386-23-3 3-((E)-4-methylstyryl)-3-((E)-styryl)cyclohexan-1-one 
• 1609386-24-4 3-((E)-4-methoxystyryl)-3-((E)-styryl)cyclohexan-1-one 
• 1609386-25-5 (E)-3-phenyl-3-styrylcyclohexan-1-one 
• 1609386-29-9 (E)-3-(3-methoxyphenyl)-3-styrylcyclohexan-1-one 
• 1609386-31-3 (E)-3-(3,5-dimethylphenyl)-3-styrylcyclohexan-1-one 
• 1609386-32-4 (E)-3-(3,5-difluorophenyl)-3-styrylcyclohexan-1-one 

Relevant academic research and scientific papers

First examples of a tosylate in the palladium-catalyzed Heck cross coupling reaction

The palladium-catalyzed cross coupling Heck reaction of tosylate (2) and methyl acrylate has been developed as an efficient method for carbon-carbon bond formation. The tosylate (2) was reacted with methyl acrylate using palladium acetate as catalyst to p

Formation of quaternary stereogenic centers by NHC-Cu-catalyzed asymmetric conjugate addition reactions with Grignard reagents on polyconjugated cyclic enones

The copper-catalyzed conjugate addition of various Grignard reagents to polyconjugated enones (dienone and enynone derivatives) is reported. The catalyst system, composed of copper triflate and an NHC ligand, led to the unusual selective formation of the 1,4-addition products. This reaction allows for the creation of all-carbon chiral quaternary centers with enantiomeric excesses up to 99 %. The remaining unsaturation on the 1,4 adducts give access to valuable synthetic transformations. Copyright

Carbonyl transposition on organoselenium compounds

Carbonyl conjugated vinylic selenides undergo 1,3 and 1,5-carbonyl transposition sequences through organometallic reagents addition reactions followed by acid hydrolysis.

Stereoselective Synthesis of Conjugated Dienones via the Palladium-Catalyzed Cross-Coupling Reaction of 1-Alkenylboronates with 3-Halo-2-alken-1-ones

The synthesis of conjugated dienones by means of palladium-catalyzed cross-coupling reaction between (E)-1-alkenyl-1,3,2-benzodioxaboroles or diisopropyl (Z)-1-hexenylboronate with 3-halo-2-alken-1-ones is described.

Reactions of 3-cyclo-2-hexenone with Carbonyl Compounds. Regio- and Chemoselective Condensations

Under the influence of SnCl4 or trimethylsilyl iodide the title compound reacts with acetals or aldehydes at the γ-position to give the corresponding condensation products, whereas fluoride or base-mediated reactions take place at the α-position to afford