Synthesis of Novel Heteroquaterphenoquinones and Their Electrochemical, Structural, and Spectroscopic Characterization
Author:
Affiliation:
1. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-77, Japan, and Biotechnology Laboratory, Sumitomo Chemical Co., Ltd., Takarazuka 665, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo9600363
Reference23 articles.
1. SYNTHESIS AND PROPERTIES OF 2-CYCLOHEPTATRIENYLIDENE-5-DICYANOMETHYLIDENE-2,5-DIHYDROTHIOPHENE (A THIOPHENE ANALOG OF [1.6.7]QUINARENE)
2. Chemistry of cyclic cross-conjugated system extended by quinonoid structure.
3. Synthesis and characterization of novel p-terphenoquinone analogs involving a central dihydrothiophenediylidene structure
4. Substituent Effects on Redox Potentials of Novel Amphoteric Terphenoquinone Analogues. Unsymmetrically Substituted 2,5-Bis(4-oxo-2,5-cyclohexadien-1-ylidene)-2,5-dihydrothiophenes
5. Novel Amphoteric 2,5-Furoquinonoid-Containingp-Terphenoquinone Analogues Giving Both a Stable Radical Anion and a Stable Radical Cation
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