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‘‘Synthesis of Phosphonate
Analogues of the Antibiotic Moenomycin A12’’
In the context of this work, C-glycosid-di- und trisaccharide-building
blocks of the antibiotic moenomycin A12
were synthesised on the basis of b-d-Galactose-pentaacetate. The starting material was
transferred in galactoheptonamide. The unit F of
the disaccharide component has all substituents,
which the unit F of the Moenomycins A12
has. The prepared synthesis way should be suitable for the synthesis of other
analogues. to the thesis (PDF-file): Summary, All, or through Leipzig University Publication Server More information is available under the research area. |
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