Journal article
Naphthopyrans by ring-closure of substituted naphthalenes using potassium t-butoxide in dimethylformamide
Journal of the Chemical Society, Perkin Transactions 1, pp.2309-2313
1983
Abstract
Two 2-alkenyl-3-hydroxyalkyl-1,4-dimethoxynaphthalenes are cyclised with potassium t-butoxide in dimethylformamide to give 3-alkyl-3,4-dihydro-5,10-dimethoxynaphtho [2,3-c] pyrans under anaerobic conditions. One of these products is treated with the same solvent and base, but in air, to give the two possible 4-hydroxy derivatives.
Details
- Title
- Naphthopyrans by ring-closure of substituted naphthalenes using potassium t-butoxide in dimethylformamide
- Authors/Creators
- R.G.F. Giles (Author/Creator)I.R. Green (Author/Creator)V.I. Hugo (Author/Creator)P.R.K. Mitchell (Author/Creator)S.C. Yorke (Author/Creator)
- Publication Details
- Journal of the Chemical Society, Perkin Transactions 1, pp.2309-2313
- Publisher
- Royal Society of Chemistry
- Identifiers
- 991005541147907891
- Copyright
- © 1983 Royal Society of Chemistry
- Murdoch Affiliation
- Murdoch University
- Language
- English
- Resource Type
- Journal article
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