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Issue 11, 1993
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Stereoselective template-directed C-glycosidation. Synthesis of bicyclic ketooxetanes via intramolecular cyclization reactions of (2-pyridylthio)glycosidic silyl enol ethers

Abstract

Bicyclic ketooxetanes 5a, 5b and 8 are formed with excellent stereoselectivity on treatment of (2-pyridylthio)glycosidic silyl enol ethers 1a, 1b and 2 with silver(I) trifluoromethanesulfonate.

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Article type: Paper
DOI: 10.1039/C39930000901
Citation: J. Chem. Soc., Chem. Commun., 1993,0, 901-903

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    Stereoselective template-directed C-glycosidation. Synthesis of bicyclic ketooxetanes via intramolecular cyclization reactions of (2-pyridylthio)glycosidic silyl enol ethers

    D. Craig and V. R. N. Munasinghe, J. Chem. Soc., Chem. Commun., 1993, 0, 901
    DOI: 10.1039/C39930000901

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