Ring-Opening Reaction of Cyclopropanated [60]Fullerenes: Unexpected Transformation of Methano[60]fullerenes Having an Electron-Donating Group on the Methano-Bridge Carbon-Reference-Cited by-同舟云学术

Ring-Opening Reaction of Cyclopropanated [60]Fullerenes: Unexpected Transformation of Methano[60]fullerenes Having an Electron-Donating Group on the Methano-Bridge Carbon

Published:2007-04-24 Issue:11 Volume:9 Page:2083-2086
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Tada Tomoyuki¹,Ishida Yasuhiro¹,Saigo Kazuhiko¹

Affiliation:

1. Department of Chemistry and Biotechnology, Graduate School of Engineering, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0705705

Reference20 articles.

1. The chemical properties of buckminsterfullerene (C60) and the birth and infancy of fulleroids

2. Syntheses, structures, and properties of methanofullerenes

3. Linear free energy relation of methanofullerene C61-substituents with cyclic voltammetry: Strong electron withdrawal anomaly

4. Macrocyclization on the fullerene core: Direct regio- and diastereoselective multi-functionalization of [60]fullerene, and synthesis of fullerene-dendrimer derivatives

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