Electrosynthesis of Symmetric and Highly Conjugated Benzofuran via a Unique ECECCC Electrochemical Mechanism: Evidence for Predominance of Electrochemical Oxidation versus Intramolecular Cyclization-Reference-Cited by-同舟云学术

Electrosynthesis of Symmetric and Highly Conjugated Benzofuran via a Unique ECECCC Electrochemical Mechanism: Evidence for Predominance of Electrochemical Oxidation versus Intramolecular Cyclization

Published:2007-04-10 Issue:10 Volume:72 Page:3646-3651
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Nematollahi Davood¹,Amani Amene¹,Tammari Esmail¹

Affiliation:

1. Faculty of Chemistry, University of Bu-Ali-Sina, Hamadan, 65174, Iran, and Asadabad Center, Payame Noor University, Iran

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo062468b

Reference19 articles.

1. Thienopyridine and benzofuran derivatives as potent anti-tumor agents possessing different structure–activity relationships

2. Major depression and the synthetic enhancer substances, (−)-deprenyl and R-(−)-1-(benzofuran-2-yl)-2-propylaminopentane

3. Two Novel Cytotoxic Benzofuran Derivatives from Brazilian Propolis

4. A new facile electrochemical method for the synthesis of 4-(pyridine-2-ylthio)benzene-l,2-diols

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