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Bingel Cycloaddition of N-Maleopimarimide-Substituted Amino-Acid Chloromethylketones to Fullerene C60

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Chemistry of Natural Compounds Aims and scope

Lipophilic conjugates of fullerene C60 were prepared via Bingel [2+1]-cycloaddition of chloromethylketones based on N-maleopimarimide-substituted amino acids to the fullerene framework.

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Acknowledgment

The work was performed according to planned research activities of Ufa Institute of Chemistry, RAS, on the topic “Synthesis of Biologically Active Heterocyclic and Terpenoid Compounds” (State Reg. No. AAAA-A17-117011910025-6). Informational support came from RFBR Grant No. 13-00-14056. The spectral part of the research used equipment at Khimiya CUC, UfIC, RAS.

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Correspondence to R. N. Malikova.

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Translated from Khimiya Prirodnykh Soedinenii, No. 3, May–June, 2018, pp. 408–412.

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Sakhautdinov, I.M., Malikova, R.N., Nugumanov, T.R. et al. Bingel Cycloaddition of N-Maleopimarimide-Substituted Amino-Acid Chloromethylketones to Fullerene C60. Chem Nat Compd 54, 481–486 (2018). https://doi.org/10.1007/s10600-018-2384-1

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  • DOI: https://doi.org/10.1007/s10600-018-2384-1

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