Synthesis of the Bicyclic Moiety of the Miharamycins by Samarium (II) Iodide Induced Ring Closure
- 1 March 1995
- journal article
- letter
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 1995 (03) , 277-279
- https://doi.org/10.1055/s-1995-4927
Abstract
The bicyclic carbohydrate moiety of miharamycins (A and B) was constructed through intramolecular reductive cyclisation of a ketosugar with an appropriate ethynic appendage.Keywords
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