136015-72-0

Upstream product

• 71813-50-8 1-bromo-2-(but-3-enyl)benzene 
• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 106-96-7 propargyl bromide 

Downstream Products

• 136015-79-7 {(E)-2-[2-(2-Bromo-phenyl)-ethyl]-pent-1-en-3-ynyl}-trimethyl-silane 
• 136015-79-7 {(Z)-2-[2-(2-Bromo-phenyl)-ethyl]-pent-1-en-3-ynyl}-trimethyl-silane 
• 83-33-0 inden-1-one 
• 710980-60-2 1-bromo-2-(7-iodo-hept-3-ynyl)-benzene 
• 710981-84-3 2-[7-(2-bromophenyl)hept-4-ynyl]maloninitrile 
• 710980-67-9 2-[7-(2-bromophenyl)hept-4-ynyl]malonic acid dimethyl ester 
• 157730-07-9 2-{(2-bromophenyl)ethyl}-3-trimethylgermyl-(Z)-prop-2-enenitrile 
• 710980-53-3 1-bromo-2-(7-chloro-hept-3-ynyl)-benzene 
• 15298-67-6 1-benzylidene-indan 

Relevant academic research and scientific papers

Aryl radical cyclization with alkyne followed by tandem carboxylation in methyl 4-tert-butylbenzoate-mediated electrochemical reduction of 2-(2-propynyloxy)bromobenzenes in?the presence of carbon dioxide

Constant current electrolysis of 2-(2-propynyloxy)bromobenzenes in DMF using an undivided cell equipped with a Pt cathode and an Mg anode in the presence of carbon dioxide and an electron transfer mediator, methyl 4-tert-butylbenzoate, resulted in aryl ra

A study on the regio- and stereoselectivity in palladium-catalyzed cyclizations of alkenes and alkynes bearing bromoaryl and nucleophilic groups

We have studied the remarkable dependence of the stereochemistry of the cyclization on the double bond geometry and of the effect of the bulkiness of the nucleophile on the regiochemistry of the palladium mediated cyclization of alkenes bearing aryl bromides and nucleophiles. In contrast, the cyclization of the acetylenic homologous substrates is not dependent on the nature of the nucleophile.