Journal article
Synthesis of a protected 2-ethoxy-3-hydroxyethylfuran and its regioselectivity as a Diels–Alder diene on reaction with 3,5-dimethoxydehydrobenzene
Arkivoc, Vol.2002(3)
2002
Abstract
As a potential route for the synthesis of naturally occurring benzisochromanequinones, 2-ethoxy-3-(1′-methoxymethoxyethyl)furan 15 was prepared and shown to react regioselectively with in situ generated 3,5-dimethoxydehydrobenzene to afford, after hydrolysis and alkylation, the target naphthalene 1-(6′,8′-dimethoxy-1′-ethoxy-4′- isopropoxy-2′-naphthalenyl)-1-(methoxymethoxy)ethane 27...
Details
- Title
- Synthesis of a protected 2-ethoxy-3-hydroxyethylfuran and its regioselectivity as a Diels–Alder diene on reaction with 3,5-dimethoxydehydrobenzene
- Authors/Creators
- R.G.F. Giles (Author/Creator) - Murdoch UniversityC.P. Taylor (Author/Creator)
- Publication Details
- Arkivoc, Vol.2002(3)
- Publisher
- Michigan Publishing
- Identifiers
- 991005540350107891
- Murdoch Affiliation
- School of Chemical and Mathematical Science
- Language
- English
- Resource Type
- Journal article
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- Citation topics
- 1 Clinical & Life Sciences
- 1.219 Cancer Drugs
- 1.219.1527 Naphthoquinone Derivatives
- Web Of Science research areas
- Chemistry, Organic
- ESI research areas
- Chemistry