SYNTHESIS OF THE BICYCLIC MOIETY OF THE MIHARAMYCINS BY SAMARIUM(II) IODIDE INDUCED RING-CLOSURE

Authors
FAIRBANKS AJ SINAY P
Citation
Aj. Fairbanks et P. Sinay, SYNTHESIS OF THE BICYCLIC MOIETY OF THE MIHARAMYCINS BY SAMARIUM(II) IODIDE INDUCED RING-CLOSURE, Synlett, (3), 1995, pp. 277-279
Citations number
30
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
3
Year of publication
1995
Pages
277 - 279
Database
ISI
SICI code
0936-5214(1995):3<277:SOTBMO>2.0.ZU;2-M
Abstract
The bicyclic carbohydrate moiety of miharamycins (A and B) was constru cted through intramolecular reductive cyclisation of a ketosugar with an appropriate ethynic appendage.