Abstract
The 1,3-dipolar cycloaddition products of C,N-disubstituted nitrones and different in situ prepared mono-N-substituted nitrones to η6-(styrene) chromium tricarbonyl and η6-(ethyl cynnamate) chromium tricarbonyl were synthesized and characterized by HPLC, IR, 1H NMR spectroscopy, and mass spectrometry. The resulted isoxazolidines were produced with a full regioselectivity and high stereoselectivity reached 100% in most cases.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2059–2064, November, 2012.
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Artemov, A.N., Sazonova, E.V., Mavrina, E.A. et al. Synthesis of new η6-(arene) chromium tricarbonyl complexes of isoxazolidines by 1,3-dipolar cycloaddition. Russ Chem Bull 61, 2076–2081 (2012). https://doi.org/10.1007/s11172-012-0290-4
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DOI: https://doi.org/10.1007/s11172-012-0290-4