Synthesis of N-substituted 4-hydroxynaphthalimides using palladium-catalysed hydroxylation


Autoria(s): Fleming, Cassandra L.; Nalder, Tim D.; Doeven, Egan H.; Barrow, Colin J.; Pfeffer, Frederick M.; Ashton, Trent D.
Data(s)

01/03/2016

Resumo

Successful implementation of a palladium-mediated hydroxylation of N-substituted 4-chloro-1,8-naphthalimides has been achieved. The methodology detailed herein utilises 4-chloro-1,8-naphthalic anhydride as a starting point and implements the catalyst/ligand combination of Pd(OAc)2/t-BuXPhos; all of which are relatively inexpensive. A range of imide substituents tolerated the reaction conditions, including acid sensitive substrates which are not compatible with other existing methodology. As such this approach is not only complimentary to existing procedures, it presents a more direct alternative to accessing 4-hydroxy-1,8-naphthalimides.

Identificador

http://hdl.handle.net/10536/DRO/DU:30082386

Idioma(s)

eng

Publicador

Elsevier

Relação

http://dro.deakin.edu.au/eserv/DU:30082386/pfeffer-synthesisofn-2016.pdf

http://www.dx.doi.org/10.1016/j.dyepig.2015.11.007

Direitos

2016, Elsevier

Palavras-Chave #Science & Technology #Physical Sciences #Technology #Chemistry, Applied #Engineering, Chemical #Materials Science, Textiles #Chemistry #Engineering #Materials Science #Palladium #Hydroxylation #Buchwald-Hartwig #4-Hydroxy-1,8-naphthalimide #Biarylphosphine #Fluorescence #RATIOMETRIC FLUORESCENT-PROBE #IMAGING HYDROGEN-SULFIDE #ARYL HALIDES #LIVING CELLS #1,8-NAPHTHALIMIDE DERIVATIVES #PHENOLS #ETHERS
Tipo

Journal Article