Straightforward and Versatile Synthesis of Fullerooxazoles from C 60  and Carboxamides through Radical Reactions under Mild Conditions | Zendy

Takeda Youhei | Zendy; Enokijima Satoru | Zendy; Nagamachi Toshiki | Zendy; Nakayama Kazuhisa | Zendy; Minakata Satoshi | Zendy

Premium

Straightforward and Versatile Synthesis of Fullerooxazoles from C 60 and Carboxamides through Radical Reactions under Mild Conditions

Author(s) -

Takeda Youhei,

Enokijima Satoru,

Nagamachi Toshiki,

Nakayama Kazuhisa,

Minakata Satoshi

Publication year - 2013

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.201200114

Subject(s) - chemistry , fullerene , oxazoline , thermostability , combinatorial chemistry , electrochemistry , solubility , organic chemistry , nanotechnology , catalysis , materials science , electrode , enzyme

A direct synthetic method for producing oxazoline‐fused fullerenes, that is, fullerooxazoles, from [60] fullerene and readily available carboxamides by radical pathways has been developed. The method presented allows efficient access to a variety of fullerooxazoles with high functional compatibility under mild reaction conditions. Furthermore, systematic investigation of their properties, such as solubility, thermostability, and electrochemical behavior, was conducted.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research