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

Lipophilic conjugates of fullerene C 60 were prepared via Bingel [2+1]-cycloaddition of chloromethylketones based on N -maleopimarimide-substituted amino acids to the fullerene framework.

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Veröffentlicht in:Chemistry of natural compounds 2018-05, Vol.54 (3), p.481-486
Hauptverfasser: Sakhautdinov, I. M., Malikova, R. N., Nugumanov, T. R., Biglova, Yu. N., Atangulov, A. B., Yunusov, M. S.
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container_end_page 486
container_issue 3
container_start_page 481
container_title Chemistry of natural compounds
container_volume 54
creator Sakhautdinov, I. M.
Malikova, R. N.
Nugumanov, T. R.
Biglova, Yu. N.
Atangulov, A. B.
Yunusov, M. S.
description Lipophilic conjugates of fullerene C 60 were prepared via Bingel [2+1]-cycloaddition of chloromethylketones based on N -maleopimarimide-substituted amino acids to the fullerene framework.
doi_str_mv 10.1007/s10600-018-2384-1
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subjects Amino acids
Buckminsterfullerene
Cycloaddition
Fullerenes
Medicine
Organic Chemistry
Pharmacy
Plant Sciences
Substitutes
title Bingel Cycloaddition of N-Maleopimarimide-Substituted Amino-Acid Chloromethylketones to Fullerene C60
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