92241-60-6

Upstream product

• 100-66-3 methoxybenzene 
• 35675-44-6 4-methylphenylacetyl chloride 
• 624-31-7 4-tolyl iodide 
• 801301-72-4 2-(2,2-bis(4-methoxyphenyl)ethenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 104-81-4 4-Methylbenzyl bromide 
• 60512-56-3 1-(2,2-dibromovinyl)-4-methylbenzene 
• 5720-07-0 4-methoxyphenylboronic acid 
• 589-18-4 4-Methylbenzyl alcohol 
• 127349-06-8 N′-(bis(4-methoxyphenyl)-methylene)-4-methylbenzenesulfonohydrazide 
• 34921-09-0 diethyl (4-methylbenzyl) phosphate 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 17792-18-6 3,3-bis(4-methoxyphenyl)propenoic acid 
• 127-09-3 sodium acetate 

Downstream Products

• 24792-49-2 trans-1,1-Bis-<4-methoxy-phenyl>-2-<4-(4-phenyl-styryl)-phenyl>-ethylen 
• 24792-50-5 trans-1,1-Bis-<4-methoxy-phenyl>-2-<4-(2-naphthyl-(2)-ethenyl)-phenyl>-ethylen 
• 24792-48-1 trans-1,1-Bis-(4-methoxy-phenyl)-2-<4-(3,4,5-trimethoxy-styryl)-phenyl>-ethylen 
• 24792-47-0 trans-1,1-Bis-(4-methoxy-phenyl)-2-<4-(3,4-dimethoxy-styryl)-phenyl>-ethylen 
• 24792-45-8 trans-1,1-Bis-(4-methoxy-phenyl)-2-<4-(4-phenoxy-styryl)-phenyl>-ethylen 
• 24792-44-7 trans-1,1-Bis-<4-methoxy-phenyl>-2-<4-styryl-phenyl>-ethylen 
• 77385-77-4 2,2-dianisyl-1-tolylvinyl bromide 
• 56074-62-5 2,2-bis-(4-methoxyphenyl)-1-p-tolylethanone 
• 92241-64-0 (E)-1,2-dianisyl-2-tolylvinyl acetate 
• 92241-65-1 (Z)-1,2-dianisyl-2-tolylvinyl acetate 

Relevant academic research and scientific papers

Pd-Catalyzed Coupling of N-Tosylhydrazones with Benzylic Phosphates: Toward the Synthesis of Di- or Tri-Substituted Alkenes

This study shows that various di- and tri-substituted alkenes with high chemoselectivity were obtained in good to high yields by coupling N-tosylhydrazones (NTHs) with benzylic phosphates as electrophilic partners. The obtained new catalytic system consis

Effective palladium-catalyzed synthesis of triarylethene-based molecules in aqueous solution

Highly effective and selective Pd-catalyzed coupling reactions of 1,1-dibromo-1-alkenes with various arylboronic acids have been performed in aqueous solution under mild conditions. The method is simple, economic, and practical for the synthesis of triarylethene-based compounds. Copyright

Rapid construction of multisubstituted olefin structures using vinylboronate ester platform leading to highly fluorescent materials

(Chemical Equation Presented) A catalytic one-pot triarylation on the C=C core of vinylboronate pinacol ester (1) produces extended π-systems based on a multisubstituted olefin structure very rapidly. We established an efficient protocol for the Pd-cataly

AMINIUM RADICAL SALT CATALYZED DESULPHURIZATION OF THIIRANES: AN EFFICIENT PREPARATION OF ARYLSUBSTITUTED OLEFINS

Arylsubstituted olefins are obtained from corresponding thiiranes in high yields under mild conditions by using catalytic amount of tris-(p-bromophenyl)aminium hexachloroantimonate (1) as a single electron transfer (SET) oxidant.

Solvolytic rearrangements of 2,2-Dianisyl-1-tolylvinyl Bromide and (E)- and (Z)-1,2-Dianisyl-2-tolylvinyl Bromide

The solvolysis of 2,2-dianisyl-1-tolylvinyl bromide (3-Br) in AcOH-AgOAc, AcOH-NaOAc, or 2,2,2-trifluoroethanol (TFE)-2,6-lutidine gave complete rearrangement to (E)- and (Z)-1,2-dianisyl-2-tolylvinyl acetates or 2,2,2-trifluoroethyl ethers, respectively,