Journal
SYNTHETIC COMMUNICATIONS
Volume 41, Issue 6, Pages 832-840Publisher
TAYLOR & FRANCIS INC
DOI: 10.1080/00397911003706982
Keywords
Arylates; ketones; Suzuki-coupling; triphenylamine; triphenylamine boronic acid
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Funding
- NSFC [60868001]
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[image omitted] A series of triphenylamine-mdified arylates and ketones were synthesized via Pd-catalyzed Suzuki coupling reaction of triphenylamine boronic acid with aryl bromide. The triphenylamine boronic acid was synthesized by iodization of 4-bromoaniline, Ullmann reaction of 1-bromo-4-iodobenzene with diphenylamine, and boronic acidification of 4-bromotriphenylamine.
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