Reactions of nitroxides XIII: Synthesis of the Morita–Baylis–Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, and DABCO and quinuclidine as catalysts

Jerzy Zakrzewski
Beilstein J. Org. Chem. 2012, 8, 1515–1522. https://doi.org/10.3762/bjoc.8.171

Supporting Information

Supporting Information features EIMS and IR spectra of the synthesized compounds 5a–o, 1H and 13C NMR of 5d with phenylhydrazine, and the chromatographic separation of 5l.

Supporting Information File 1: Detailed spectrographic data.
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Reactions of nitroxides XIII: Synthesis of the Morita–Baylis–Hillman adducts bearing a nitroxyl moiety using 4-acryloyloxy-2,2,6,6-tetramethylpiperidine-1-oxyl as a starting compound, and DABCO and quinuclidine as catalysts
Jerzy Zakrzewski
Beilstein J. Org. Chem. 2012, 8, 1515–1522. https://doi.org/10.3762/bjoc.8.171

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Zakrzewski, J. Beilstein J. Org. Chem. 2012, 8, 1515–1522. doi:10.3762/bjoc.8.171

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