Chemoselectivity in the reaction of metal phenolates with aromatic dialdehydes
- 1 January 1994
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 13,p. 1879-1882
- https://doi.org/10.1039/p19940001879
Abstract
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).Keywords
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