Facile and reversible synthesis of an acidic water-soluble poly(amidoamine) fullerodendrimer

Yutaka Takaguchi, Yuuki Sako, Yasushi Yanagimoto, Sadao Tsuboi, Jiro Motoyoshiya, Hiromu Aoyama, Takatsugu Wakahara, Takeshi Akasaka

Research output: Contribution to journal › Article

50 Citations (Scopus)

Abstract

Water-soluble fullerodendrimer was obtained by the use of a Diels-Alder reaction of C60 with a newly designed anthryl dendron under an extremely mild condition in 70% yield, which is more than five times as high as the yield described in our previous report.

Original languageEnglish
Pages (from-to)5777-5780
Number of pages4
JournalTetrahedron Letters
Volume44
Issue number31
DOIs
Publication statusPublished - Jul 28 2003

Keywords

  • Anthracene
  • Cycloaddition
  • Fullerodendrimer
  • Water-soluble fullerene

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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    Takaguchi, Y., Sako, Y., Yanagimoto, Y., Tsuboi, S., Motoyoshiya, J., Aoyama, H., Wakahara, T., & Akasaka, T. (2003). Facile and reversible synthesis of an acidic water-soluble poly(amidoamine) fullerodendrimer. Tetrahedron Letters, 44(31), 5777-5780. https://doi.org/10.1016/S0040-4039(03)01425-4