Chemical and electrochemical reduction of the products from the reactions of isoindolines and tetracyanoethylene
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference29 articles.
1. Electron Spin Resonance of Electrolytically Generated Nitrile Radicals
2. 11,11,12,12-Tetracyano-1,4-naphthaquinodimethane: a new electron acceptor
3. Improved synthetic route to 11, 11, 12, 12-tetracyanonaphtho-2,6-quinodimethan
4. Synthesis of 13,13,14,14-tetracyanopyreno-2,7-quinodimethane, an electron acceptor for organic metals
5. Synthesis and electrochemical properties of 15,15,16,16-tetracyano-6, 13-pentacenequinodimethane (TCPQ)
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1. Novel Synthesis of 1,3-Thiazine and Pyrimidinethione Derivatives from (1-Aryl ethylidene)hydrazinecarbothioamides and Tetracyanoethylene;Journal of Heterocyclic Chemistry;2015-07-02
2. Electrochemical Behavior of Some Substituted Thiosemicarbazones and their Reaction Products with Tetracyanoethylene;International Journal of Electrochemical Science;2008
3. 15.3.2 Nitrogen containing heterocycles;Landolt-Börnstein - Group II Molecules and Radicals;2008
4. New reaction of ethenetetracarbonitrile with N-arylisoindolines;Tetrahedron;2003-06
5. A novel reaction of (2a7-trinito-9H-fluoren-9-ylidene)-propanedinitrile withN-arylisoindolines;Journal of Heterocyclic Chemistry;1998-01
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