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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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