Journal article
Mercury(II) mediated cyclisation of R-1-(1′-hydroxyethyl)-2-(1″-propenyl)-3-alkoxy-4-methoxybenzenes to chiral isochromanes
Tetrahedron, Vol.60(11), pp.2629-2637
2004
Abstract
A protocol has been established for the transformation of chiral ortho 1-hydroxyethyl propenyl benzenes under both anaerobic and oxidative mercury(II) mediated conditions to produce chiral isochromanes. Further transformations of the former products yielded chiral isochromanquinones, while the latter afforded the corresponding chiral 4-hydroxyisochromanquinones.
Details
- Title
- Mercury(II) mediated cyclisation of R-1-(1′-hydroxyethyl)-2-(1″-propenyl)-3-alkoxy-4-methoxybenzenes to chiral isochromanes
- Authors/Creators
- C.B. de Koning (Author/Creator)R.G.F. Giles (Author/Creator)I.R. Green (Author/Creator)N.M. Jahed (Author/Creator)
- Publication Details
- Tetrahedron, Vol.60(11), pp.2629-2637
- Publisher
- Elsevier
- Identifiers
- 991005540192107891
- Copyright
- © 2004 Elsevier Ltd
- Murdoch Affiliation
- Murdoch University
- 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