Rediscovering the double Friedel-Crafts acylation : an expedient entry to phenanthrene-9,10-diones


Autoria(s): Crosta, Nicoletta; Müller, Sebastian; Gradl, Dietmar; Masters, Kye-Simeon; Bräse, Stefan
Data(s)

2013

Resumo

The double Friedel–Crafts acylation of readily accessible biaryls with oxalyl chloride delivers the respective phenanthrene-9,10-diones, providing an alternative to the traditional methods, which require harsh oxidizing conditions and multistep sequences. This simple method allows the synthesis of various symmetrical and non-symmetrical targets, and is even effective for the synthesis of the parent ring system from (unactivated) biphenyl.

Identificador

http://eprints.qut.edu.au/69690/

Publicador

Georg Thieme Verlag

Relação

DOI:10.1055/s-0032-1318481

Crosta, Nicoletta, Müller, Sebastian, Gradl, Dietmar, Masters, Kye-Simeon, & Bräse, Stefan (2013) Rediscovering the double Friedel-Crafts acylation : an expedient entry to phenanthrene-9,10-diones. Synlett, 24(8), pp. 951-954.

Direitos

Copyright 2013 Georg Thieme Verlag

Fonte

School of Chemistry, Physics & Mechanical Engineering; Science & Engineering Faculty

Palavras-Chave #030503 Organic Chemical Synthesis
Tipo

Journal Article