Tricyanovinylation of 2-aryl-1-vinylpyrroles: solvent- and substituent controlled chemo- and regioselectivity-Reference-Cited by-同舟云学术

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Tricyanovinylation of 2-aryl-1-vinylpyrroles: solvent- and substituent controlled chemo- and regioselectivity

Published:2009-05 Issue:22 Volume:65 Page:4326-4331
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Trofimov Boris A.,Sobenina Lyubov' N.,Drichkov Vladislav N.,Ushakov Igor' A.,Mikhaleva Al'bina I.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference21 articles.

1. Electrochemical investigation into the interaction between various pyrrole moieties and the well-known electron acceptor, tetracyanoethylene

2. Synthesis of tricyanovinyl-substituted thienylpyrroles and characterization of the solvatochromic, electrochemical and non-linear optical properties

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Redirecting a Diels–Alder Reaction toward (2 + 2)-Cycloaddition;The Journal of Organic Chemistry;2021-02-25

2. Copper-catalyzed β-Iodovinylation of Azole and Pyrrole Derivatives;HETEROCYCLES;2020

3. Tetracyanoethylene as a mediator and building block in synthesis of 5-substituted amino-1,3,4-thiadiazolyl-1H-pyrazole derivatives;Tetrahedron Letters;2016-01

4. Addition Reactions: Cycloaddition;Organic Reaction Mechanisms Series;2011-12-06

5. Synthesis and Chromic Behaviors of Dithienosiloles with Push-Pull Substituents Toward VOC Detection;Molecular Crystals and Liquid Crystals;2010-10-08

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