Literature DB >> 21302952

Aziridinofullerene: a versatile platform for functionalized fullerenes.

Masakazu Nambo1, Yasutomo Segawa, Kenichiro Itami.   

Abstract

An aziridine moiety on the fullerene core can serve as an acid-triggered reacting template for the controlled synthesis of a range of functionalized fullerenes that are otherwise difficult to synthesize in an efficient and selective manner. A copper-catalyzed aziridination of C(60) for the practical synthesis of aziridinofullerene 1 and acid-catalyzed reactions of 1 with mono- and bifunctional nucleophiles as well as alkynes are described. The rapid generation of structural diversity in a single chemical operation using the common platform 1 is notable.

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Year:  2011        PMID: 21302952     DOI: 10.1021/ja111213k

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  1 in total

Review 1.  Chemistry of fullerene epoxides: synthesis, structure, and nucleophilic substitution-addition reactivity.

Authors:  Yusuke Tajima; Kazumasa Takeshi; Yasuo Shigemitsu; Youhei Numata
Journal:  Molecules       Date:  2012-05-25       Impact factor: 4.411

  1 in total

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