92434-54-3

Upstream product

• 36901-75-4 (2-bromobenzyl)triphenylphosphonium bromide 
• 123-11-5 4-methoxy-benzaldehyde 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 6630-33-7 ortho-bromobenzaldehyde 

Downstream Products

• 937634-53-2 1-bromo-2-(4-methoxyphenethyl)benzene 
• 937643-47-5 4-(2-bromophenethyl)phenol 
• 27884-09-9 2-(4-methoxyphenyl)benzo[b]thiophene 
• 1608105-74-3 C₁₉H₂₀O₄ 
• 1608105-90-3 C₂₃H₂₀O₄ 
• 1608105-82-3 C₁₇H₁₆O₄ 
• 1608105-38-9 1,1-dimethyl 2-phenyl 2-(2-(4-methoxyphenylethyl)phenyl)ethene-1,1,2-tricarboxylate 
• 1111311-21-7 ethyl 3-(4-methoxybenzyl)-2H-isoindole-1-carboxylate 
• 1111310-64-5 ethyl (Z)-2-hydroxy-2-(2-(4-methoxystyryl)phenyl)acetate 
• 1111310-91-8 ethyl (Z)-2-(2-(4-methoxystyryl)phenyl)-2-(methylsulfonyloxy)acetate 

Relevant academic research and scientific papers

Photochemistry of o-pyrrolylstilbenes and formation of spiro-2H-pyrroles and their rearrangement to dihydroindoles

(Chemical Equation Presented) Excited states of stilbenylpyrroles 1a-1c deactivate by two photochemical processes: cis-trans-isomerization and hydrogen transfer of NH to the stilbene double bond. NH-transfer results in the formation of two quinone dimetha

Catalytic enantioselective C(sp3)H functionalization: Intramolecular benzylic [1,5]-hydride shift

The catalytic asymmetric [1,5]-hydride transfer/cyclization sequence involving benzylic C(sp3)H bond was established, providing tetrahydronaphthalene derivatives in moderate to high yield with up to 69% ee, by employing the copper complex of si

Palladium(0)-catalyzed arylative dearomatization of phenols

The palladium-catalyzed arylative dearomatization of phenols to yield spirocyclohexadienone products in good to excellent yields has been developed. Preliminary results demonstrate that the formation of the spirocyclic all-carbon quaternary center can be accomplished with high levels of enantiocontrol (up to 91% ee).

Orthogonal synthesis of isoindole and isoquinoline derivatives from organic azides

(Chemical Equation Presented) α-Azido carbonyl compounds bearing a 2-alkenylaryl moiety at the α-position are found to be promising precursors for synthesis of isoindole and isoquinoline derivatives via 1,3-dipolar cycloaddrtion of azides onto alkenes and fcrelectrocyclization of N-H imine intermediates, respectively.