>
Fa   |   Ar   |   En
   Regioselective synthesis of anilines and β-dibrominated acetamides from N-aryl acetoacetamides mediated by Cu(I) salts  
   
نویسنده tan l.-q. ,liu w.-b. ,zhou p. ,chen c. ,zhang q.
منبع journal of saudi chemical society - 2016 - دوره : 20 - شماره : 2 - صفحه:220 -226
چکیده    A highly regioselective synthetic strategy mediated by cu(i) salts is presented for the synthesis of anilines and β-dibrominated acetamides from n-aryl acetoacetamides. a variety of n-aryl acetoacetamides were used in this protocol,and a wide range of polysubstituted anilines and β-dibrominated acetamides were obtained in moderate to good yields. when employing cui as the additive in this strategy,anilines are obtained,however,when using cubr as the partner of cui under a mild condition,β-dibrominated acetamides are afforded. © 2014 king saud university.
کلیدواژه Anilines; Cleavage of carbon-carbon bond; Cleavage of carbon-nitrogen bond; Regioselective synthesis; β-Dibrominated acetamides
آدرس school of chemistry and life science,guangdong university of petrochemical technology,2 guandu road, China, school of chemistry and life science,guangdong university of petrochemical technology,2 guandu road, China, school of chemistry and life science,guangdong university of petrochemical technology,2 guandu road, China, school of chemistry and life science,guangdong university of petrochemical technology,2 guandu road, China, school of chemistry and life science,guangdong university of petrochemical technology,2 guandu road, China
 
     
   
Authors
  
 
 

Copyright 2023
Islamic World Science Citation Center
All Rights Reserved