Catalog Home Page

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.

[img]
Preview
PDF - Published Version
Download (126kB) | Preview
Free to read: http://dx.doi.org/10.3998/ark.5550190.0003.911
*No subscription required

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.

Publication Type: Journal Article
Murdoch Affiliation: 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
Item Control Page Item Control Page

Downloads

Downloads per month over past year