DETERMINATION OF THE ABSOLUTE STEREOCHEMISTRY AT THE C16 ORTHOESTER OF EVERNINOMICIN ANTIBIOTICS; A NOVEL ACID-CATALYZED ISOMERIZATION OF ORTHOESTERS
- 1 November 1997
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (46) , 7989-7992
- https://doi.org/10.1016/s0040-4039(97)10178-2
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Complete1H and13C NMR Assignments of the Oligosaccharide Antibiotic Sch 27899Magnetic Resonance in Chemistry, 1997
- The Structure of New Oligosaccharide Antibiotics, 13-384 Components 1 and 5HETEROCYCLES, 1989
- Synthesis of the disaccharide CD fragment found in everninomicin-C and -D, avalamycin-A and -C and curamycin-A: stereochemistry at the spiro-ortholactone centerTetrahedron Letters, 1987
- The orthosomycins, a new family of antibioticsTetrahedron, 1979
- X-Ray crystal and molecular structure of olgose, a major degradation product of the oligosaccharide antibiotic everninomicin DJournal of the Chemical Society, Chemical Communications, 1979
- Structure of everninomicin DJournal of the American Chemical Society, 1975
- Structure of everninomicin C.The Journal of Antibiotics, 1975
- Structure of evernnomicin B.The Journal of Antibiotics, 1975