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Molecules ; 23(11)2018 Nov 03.
Article in English | MEDLINE | ID: mdl-30400283

ABSTRACT

A new synthesis of substituted acridines is achieved by palladium-catalyzed addition of terminal acetylenes between the aryl rings of bis(2-bromophenyl)amine. By including a diamine base and elevating the temperature, the reaction pathway favors the formation of acridine over a double Sonogashira reaction to form bis(tolan)amine. This method is demonstrated with several aryl-alkynes and alkyl-alkynes.


Subject(s)
Acridines/chemistry , Acridines/chemical synthesis , Amines/chemistry , Alkynes/chemistry , Molecular Structure , Temperature
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