Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans – an approach to carbohydrate mimetics

Fabian Pfrengle and Hans-Ulrich Reissig
Beilstein J. Org. Chem. 2010, 6, No. 75. https://doi.org/10.3762/bjoc.6.75

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Supporting Information File 1: Experimental procedures, characterization data, 1H NMR and 13C NMR spectra of synthesized compounds.
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Addition of lithiated enol ethers to nitrones and subsequent Lewis acid induced cyclizations to enantiopure 3,6-dihydro-2H-pyrans – an approach to carbohydrate mimetics
Fabian Pfrengle and Hans-Ulrich Reissig
Beilstein J. Org. Chem. 2010, 6, No. 75. https://doi.org/10.3762/bjoc.6.75

How to Cite

Pfrengle, F.; Reissig, H.-U. Beilstein J. Org. Chem. 2010, 6, No. 75. doi:10.3762/bjoc.6.75

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