Stereochemistry of alternating polyol chains: 13C NMR analysis of 1,3-diol acetonides
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (7), 945-948
- https://doi.org/10.1016/s0040-4039(00)94399-5
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Complete stereostructure of nystatin A1: A proton NMR studyTetrahedron Letters, 1989
- Stereostructure of nystatin A1: A synthetic assignment of the C1–C10 fragmentTetrahedron Letters, 1989
- A convergent synthesis of polyol chainsThe Journal of Organic Chemistry, 1989
- Microbial products. 9. Roxaticin, a new oxo pentaene antibioticThe Journal of Organic Chemistry, 1989
- Stereochemical studies on the polyene macrolide nystatin A1: the hydroxyl groups in the C-1—C-10 fragment are all-synTetrahedron Letters, 1988
- Application of the two-directional chain synthesis strategy to the first stereochemical assignment of structure to members of the skipped-polyol polyene macrolide class: mycoticin A and BJournal of the American Chemical Society, 1987
- Stereochemical studies of polyols from the polyene macrolide lienomycinThe Journal of Organic Chemistry, 1987
- Determination of the stereostructure of the .DELTA.-lactones of 5,7-dihydroxy-2,3-unsaturated acids by 1H NMR spectroscopy.CHEMICAL & PHARMACEUTICAL BULLETIN, 1987
- A Review on the Conformational Aspects in the 1,3-Dioxane SystemHETEROCYCLES, 1976
- Structure and absolute configuration of the polyene macrolide antibiotic amphotericin BTetrahedron Letters, 1970