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Syntheses of asymmetric 2-benzopyrans. The influence of aromatic halogen substituents on the intramolecular cyclisation of enantiopure tethered phenolic lactaldehydes

Giles, R.G.F., Green, I.R., Oosthuizen, F.J. and Taylor, C.P. (2002) Syntheses of asymmetric 2-benzopyrans. The influence of aromatic halogen substituents on the intramolecular cyclisation of enantiopure tethered phenolic lactaldehydes. Arkivoc, IX . pp. 99-116.

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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.

Item Type: Journal Article
Murdoch Affiliation(s): School of Mathematical and Physical Sciences
Publisher: Michigan Publishing
Copyright: © 2002 ARKAT USA, Inc
Other Information: Issue in Honor of Prof. James Bull
URI: http://researchrepository.murdoch.edu.au/id/eprint/35931
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