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Selective acylation of oxygenated naphthalenes

By R.G.F. Giles, S.C. Yorke, I.R. Green and V.I. Hugo

Abstract

The synthesis of 1,4,5,7-teetraoxygenated naphthalenes is described, as well as their selective acylation at either C-3 or C-8 using either trifluoroacetic anhydride or acetic acid and trifluoroacetic anhydride; the potential of these reactions in the synthesis of naturally occurring naphthoquinones is referred to

Publisher: Chemical Society
Year: 1984
OAI identifier: oai:researchrepository.murdoch.edu.au:35672
Provided by: Research Repository
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