Journal article
Syntheses of asymmetric 2-benzopyrans. The influence of aromatic halogen substituents on the intramolecular cyclisation of enantiopure tethered phenolic lactaldehydes
Arkivoc, Vol.IX, pp.99-116
2002
Abstract
The syntheses of enantiopure brominated and chlorinated phenolic lactaldehydes are described as well as an investigation into their cyclisation to form the corresponding 2-benzopyran-4,5-diols. It is found that the choice of halogen is important in these processes.
Details
- Title
- Syntheses of asymmetric 2-benzopyrans. The influence of aromatic halogen substituents on the intramolecular cyclisation of enantiopure tethered phenolic lactaldehydes
- Authors/Creators
- R.G.F. Giles (Author/Creator)I.R. Green (Author/Creator)F.J. Oosthuizen (Author/Creator)C.P. Taylor (Author/Creator)
- Publication Details
- Arkivoc, Vol.IX, pp.99-116
- Publisher
- Michigan Publishing
- Identifiers
- 991005544351007891
- Copyright
- © 2002 ARKAT USA, Inc
- Murdoch Affiliation
- School of Mathematical and Physical Sciences
- Language
- English
- Resource Type
- Journal article
- Additional Information
- Issue in Honor of Prof. James Bull
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