A 1,2,3,4‐Tetrahydrofullerene Derivative Generated from a [60]Fulleroindoline: Regioselective Electrosynthesis and Computational Study | Zendy

Xiao Yang | Zendy; Wang Guanwu | Zendy

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A 1,2,3,4‐Tetrahydrofullerene Derivative Generated from a [60]Fulleroindoline: Regioselective Electrosynthesis and Computational Study

Author(s) -

Xiao Yang,

Wang Guanwu

Publication year - 2014

Publication title -

chinese journal of chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.28

H-Index - 41

eISSN - 1614-7065

pISSN - 1001-604X

DOI - 10.1002/cjoc.201400205

Subject(s) - regioselectivity , electrosynthesis , chemistry , derivative (finance) , fullerene , electrochemistry , surface modification , computational chemistry , combinatorial chemistry , organic chemistry , catalysis , electrode , financial economics , economics

A 1,2,3,4‐tetrahydro[60]fullerene with a five‐membered heterocycle fused to a [5,6] junction was obtained with high regioselectivity by electrochemical functionalization of a [60]fulleroindoline. The structure was determined by spectroscopic data. A plausible reaction mechanism supported by computational calculations is proposed.

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