52498-18-7

Upstream product

• 52498-17-6 1,4-Bis-(p-anisyl)-1,4-dichlor-butan 
• 5720-07-0 4-methoxyphenylboronic acid 
• 93296-09-4 4-methoxyphenylzinc chloride 
• 15982-64-6 1,4-bis(4-methoxyphenyl)butane-1,4-dione 
• 2881-83-6 ethyl 4-methoxybenzoylacetate 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 52498-16-5 1,4-bis-(4-methoxy-phenyl)-butane-1,4-diol 

Downstream Products

• 52498-14-3 cis-1,2-bis(4-methoxyphenyl)cyclobutane 
• 222158-58-9 [(1S,2R,3S,4R)-3-Hydroxymethyl-1,4-bis-(4-methoxy-phenyl)-bicyclo[2.2.0]hex-2-yl]-methanol 
• 222158-60-3 (1R,7S,8R,11S)-8,11-Bis-(4-methoxy-phenyl)-3,5-dioxa-4-thia-tricyclo[5.4.0.0^8,11]undecane 4,4-dioxide 
• 114396-02-0 (1S,4R,5R,6R)-1,4-Bis-(4-methoxy-phenyl)-5,6-dimethyl-2,3-dioxa-bicyclo[2.2.2]octane 
• 114395-98-1 (E,E)-3,6-bis(p-methoxyphenyl)-2,6-octadiene 
• 114395-97-0 (Z,Z)-3,6-bis(p-methoxyphenyl)-2,6-octadiene 

Relevant academic research and scientific papers

Substrate-Controlled Regioselective Bromination of 1,2-Disubstituted Cyclobutenes: An Application in the Synthesis of 2,3-Disubstituted Cyclobutenones

Easily available disubstituted cyclobutenes were regioselectively halogenated at the allylic position by means of a reaction with bromine. The regioselectivity of bromination is controlled by the presence of a carbocation-stabilizing group. The prepared d