Journal article
Selective acylation of oxygenated naphthalenes
Journal of the Chemical Society, Chemical Communications, (8)
1984
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.
Details
- Title
- Selective acylation of oxygenated naphthalenes
- Authors/Creators
- R.G.F. Giles (Author/Creator)S.C. Yorke (Author/Creator)I.R. Green (Author/Creator)V.I. Hugo (Author/Creator)
- Publication Details
- Journal of the Chemical Society, Chemical Communications, (8)
- Publisher
- Chemical Society
- Identifiers
- 991005540997207891
- Copyright
- © 1984 Royal Society of Chemistry
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
Metrics
16 Record Views