Synthesis of a conjugate of (R)-2,2-dichloro- N-(1-phenylethyl)acetamide with fullerene C60 View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-10

AUTHORS

S. A. Torosyan, Yu. N. Biglova, Z. F. Nuriakhmetova, M. S. Miftakhov

ABSTRACT

The Bingel–Hirsch reaction of (R)-2,2-dichloro-N-(1-phenylethyl)acetamide with fullerene C60 gave the corresponding methanofullerene, and its electrochemical and physical properties were studied. The electron-acceptor characteristics of the new compound were found to be similar to those of the known methanofullerene [60]PCBM.

PAGES

1583-1585

References to SciGraph publications

  • 2015-03. Polynorbornenes modified by methanofullerene and 1-phenyltetrazol-5-ylsulfanylmethyl blocks in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2015-08. Lipophilic fullerenes in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2016-04. Synthesis of chloramphenicol conjugate with fullerene C60 in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • 2012-05. Esters of dichloroacetic acid in the synthesis of fullerene C60 functionalized methane derivatives in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
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