Journal article
Products of an Acetylation Protocol on two Pentaalkoxynaphthalenes
Synthetic Communications, Vol.36(12), pp.1695-1706
2006
Abstract
The benzyl and isopropyl groups were evaluated as O‐protecting entities in 1,2,4,5,8‐pentaalkoxynaphthalene systems upon treatment with a proven acetylation protocol. Only the benzyl group demonstrated moderate stability.
Details
- Title
- Products of an Acetylation Protocol on two Pentaalkoxynaphthalenes
- Authors/Creators
- R.G.F. Giles (Author/Creator) - Murdoch UniversityI.R. Green (Author/Creator) - University of the Western CapeN. van Eeden (Author/Creator) - University of the Western Cape
- Publication Details
- Synthetic Communications, Vol.36(12), pp.1695-1706
- Publisher
- Taylor and Francis
- Identifiers
- 991005543378307891
- Copyright
- 2006 Taylor & Francis Group, LLC
- Murdoch Affiliation
- School of Chemical and Mathematical Science
- Language
- English
- Resource Type
- Journal article
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- Collaboration types
- Domestic collaboration
- International collaboration
- 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