Journal article
Regioselectivity in the reactions of methoxydehydrobenzenes with furans. Part 2. 2-Methoxyfuran and methoxydehydrobenzenes
Journal of the Chemical Society, Perkin Transactions 1, (6), pp.1581-1587
1991
Abstract
Acid-induced ring opening of adducts of furan and methoxydehydrobenzenes gives the naphthalenols derived from the more stable carbocation. The cycloadditions of methoxydehydrobenzenes containing a 3-methoxy group and 2-methoxyfuran are highly regiospecific. The adducts, being strained acetals, undergo ring opening to provide a convenient synthesis of naphthalenols.
Details
- Title
- Regioselectivity in the reactions of methoxydehydrobenzenes with furans. Part 2. 2-Methoxyfuran and methoxydehydrobenzenes
- Authors/Creators
- R.G.F. Giles (Author/Creator)A.B. Hughes (Author/Creator)M.V. Sargent (Author/Creator)
- Publication Details
- Journal of the Chemical Society, Perkin Transactions 1, (6), pp.1581-1587
- Publisher
- Royal Society of Chemistry
- Identifiers
- 991005543115207891
- Murdoch Affiliation
- School of Mathematical and Physical Sciences
- Language
- English
- Resource Type
- Journal article
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