Oxophilic metal phenolates undergo highly selective condensations with aromatic dialdehydes to produce compounds 6, 7, 11 and 12 resulting from di- or tetra-attack, depending upon the phenolaldehyde molar ratio. 1,4-Anthraquinones 17 were synthesized by allowing 1,4-hydroquinones to react with phthalaldehyde (OPA).
G. Sartori, F. Bigi, R. Maggi, A. Pastorio, C. Porta and G. Bonfanti, J. Chem. Soc., Perkin Trans. 1, 1994, 1879 DOI: 10.1039/P19940001879
To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.
If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.
If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.
Read more about how to correctly acknowledge RSC content.
Please wait while we load your content...