Journal article
Asymmetric syntheses of Isochroman-4,7-diols through intramolecular cyclization of tethered lactaldehydes
Australian Journal of Chemistry, Vol.53(4), pp.341-347
2000
Abstract
Ready cyclization through silica gel chromatography of the asymmetric phenolic lactaldehyde (14) afforded the diastereomeric pair of isochroman-4,7-diols (21) and (23) in good yield, while (17), the benzylic epimer of (14), similarly yielded the isochroman-4,7-diol (25) as a single diastereomer.
Details
- Title
- Asymmetric syntheses of Isochroman-4,7-diols through intramolecular cyclization of tethered lactaldehydes
- Authors/Creators
- R.G.F. Giles (Author/Creator)I.R. Green (Author/Creator)Y. Gruchlik (Author/Creator)F.J. Oosthuizen (Author/Creator)
- Publication Details
- Australian Journal of Chemistry, Vol.53(4), pp.341-347
- Publisher
- Commonwealth Scientific and Industrial Research Organization Publishing
- Identifiers
- 991005544887407891
- Copyright
- © 2000 CSIRO
- Murdoch Affiliation
- School of Chemical and Mathematical Science
- Language
- English
- Resource Type
- Journal article
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