21757-10-8

Upstream product

• 101018-40-0 1,1-bis(4-methoxyphenyl)prop-2-en-1-ol 
• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 90-96-0 bis(p-methoxyphenyl)methanone 
• 728-87-0 4,4'-Dimethoxybenzhydrol 
• 123-11-5 4-methoxy-benzaldehyde 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 22867-08-9 (E)-1-(4-Methoxy-phenyl)-4-phenyl-but-2-ene-1,4-dione 
• 100-66-3 methoxybenzene 

Relevant academic research and scientific papers

UV light-mediated difunctionalization of alkenes through aroyl radical addition/1,4-/1,2-Aryl shift cascade reactions

UV light-mediated difunctionalization of alkenes through an aroyl radical addition/1,4-/1,2-aryl shift has been described. The resulted aroyl radical from a photocleavage reaction added to acrylamide compounds followed by cyclization led to the formation of oxindoles, whereas the addition to cinnamic amides aroused a unique 1,4-aryl shift reaction. Furthermore, the difunctionalization of alkenes of prop-2-en-1-ols was also achieved through aroyl radical addition and a sequential 1,2-aryl shift cascade reaction.