The Generation of Aryl Anions by Double Electron Transfer to Aryl Iodides from a Neutral Ground-State Organic Super-Electron Donor-Reference-Cited by-同舟云学术

The Generation of Aryl Anions by Double Electron Transfer to Aryl Iodides from a Neutral Ground-State Organic Super-Electron Donor

Published:2007-07-02 Issue:27 Volume:119 Page:5270-5275
ISSN:0044-8249
Container-title:Angewandte Chemie
language:de
Short-container-title:Angew. Chem.

Author:

Murphy John A.,Zhou Sheng-ze,Thomson Douglas W.,Schoenebeck Franziska,Mahesh Mohan,Park Stuart R.,Tuttle Tell,Berlouis Leonard E. A.

Publisher

Wiley

Subject

General Medicine

Reference45 articles.

1. Can Single-Electron Transfer Break an Aromatic Carbon−Heteroatom Bond in One Step? A Novel Example of Transition between Stepwise and Concerted Mechanisms in the Reduction of Aromatic Iodides

2. Cathodic reduction of N-(2-iodophenyl)-N-alkylcinnamides: a novel sequential electrochemical radical cyclisation and hydroxylation

3. Application of a new kinetic method in the investigation of cleavage reactions of haloaromatic radical anions†

4. Much more stabilized trifluoromethyl and benzylic anions can be formed using the commercially available reagent tetrakisdimethylaminoethene (TDAE), but we have shown that that reagent does not react with aryl halides (M. Mohan, PhD thesis, University of Strathclyde, 2005);

5. Nucleophilic Trifluoromethylation Using Trifluoromethyl Iodide. A New and Simple Alternative for the Trifluoromethylation of Aldehydes and Ketones

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