Synthesis of 16-membered ring macrolide antibiotics I. Stereoselective construction of the ‘right wing” of the carbomycins and leucomycins from D-glucose
- 31 December 1979
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 20 (25) , 2327-2330
- https://doi.org/10.1016/s0040-4039(01)93964-4
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Synthesis of carbomycin B. Introduction of the amino disaccharide onto the 16-membered-ring aglyconeJournal of the American Chemical Society, 1977
- Chemical and biological studies on 16-membered macrolide antibiotics.The Journal of Antibiotics, 1975
- Conjugate addition reactions with lithium diallylcuprateThe Journal of Organic Chemistry, 1969
- The introduction of unsaturated linkages into some carbohydrates by pyrolysis of cyclic, orthoformic estersCarbohydrate Research, 1968
- Preparation of Organolithium Compounds by the Transmetalation Reaction. III. Allyllithium and Methallyllithium1,2aThe Journal of Organic Chemistry, 1961
- A SYNTHESIS OF 5,6-DIDEOXY-D-XYLOHEXOSE(5-DEOXY-5-C-METHYL-D-XYLOSE)Canadian Journal of Chemistry, 1957