2958-55-6

Upstream product

• 93-17-4 3,4-dimethoxyphenylacetonitrile 
• 100-51-6 benzyl alcohol 
• 2460-33-5 3,4-dimethoxyphenylpyruvic acid 
• 100-52-7 benzaldehyde 

Downstream Products

• 1346463-55-5 4-(3,4-dimethoxyphenyl)-5-phenylpenta-(2E,4Z)-dienoyl azide 
• 1346463-42-0 4-(3,4-dimethoxyphenyl)-5-phenylpenta-(2E,4Z)-dienoic acid 
• 1346463-30-6 (E)-2-(3,4-dimethoxyphenyl)-3-phenylacrylaldehyde 
• 1346463-83-9 (Z)-2-(3,4-dimethoxyphenyl)-3-phenylacrylaldehyde 
• 1346463-69-1 1(E)-benzylidene-5,6-dimethoxy-1H-indene 
• 1357078-99-9 4-(3,4-dimethoxyphenyl)-3-phenylpyridin-2(1H)-one 

Relevant academic research and scientific papers

Manganese Catalyzed α-Olefination of Nitriles by Primary Alcohols

Catalytic α-olefination of nitriles using primary alcohols, via dehydrogenative coupling of alcohols with nitriles, is presented. The reaction is catalyzed by a pincer complex of an earth-abundant metal (manganese), in the absence of any additives, base, or hydrogen acceptor, liberating dihydrogen and water as the only byproducts.

Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: Mechanistic studies

The thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates 1, generated in situ from the corresponding azides, was investigated using iodine as a catalyst. Diphenylpyridinones 2, phenylnaphthalenes 3, and indenes 4 were produced via intramolecular ring closure. The nature of the substituents on the phenyl rings was found to be crucial to the distribution of cyclized products 2 - 4. The mechanism of the reaction is also discussed.

Synthesis, characterisation and photophysical properties of a,a-diaryl-acrylonitrile derivatives

a,b-Diarylacrylonitrile derivatives can be prepared by two different routes: (1) the intermolecular condensation of the same arylacetonitriles (2) the condensation of arylaldehydes and arylacetonitriles with a catalytic amount of NaOCH3 at room temperature. Several a,b-diarylacrylonitrile derivatives have been synthesised in this paper and characterised. The UV-vis absorption and photoluminescent (PL) spectra of the products were investigated.

Intramolecular Biaryl Oxidative Coupling of Stilbenes by Vanadium Oxytrichloride (VOCl3): Facile Synthesis of Substituted Phenanthrene Derivatives

Vanadium oxytrichloride (VOCl3) has proven to be a highly efficient reagent for intramolecular biaryl oxidative coupling reaction of electron-rich stilbenes. Accordingly, a mild and efficient route to phenanthrene derivatives from stilbenes oxy

Stilbene derivative and stilbene analog derivative, and use thereof

The present invention relates to a novel compound having a 12-lipoxygenase inhibitory effect, of the general formula (I), a precursor thereof, and a medicine containing the same, STR1 wherein R1 represents a hydrogen atom or a hydroxy group; on