An efficient preparation and spectroscopic and electrochemical properties of quinodimethane derivatives with four 3-(methoxycarbonyl)azulen-1-yl groups

Tetrahedron

Volumn 64, Issue 17, 2008, Pages 3802-3812

  Takekuma, Shin ichi ^a   Sonoda, Kazutaka ^a   Minematsu, Toshie ^a   Takekuma, Hideko ^a  

^a KINKI UNIVERSITY   (Japan)

Author keywords

Azulenes; Dicarbenium ions; Electrochemical behavior; Quinodimethanes; Spectroscopic properties; Zinc reductions

Indexed keywords

1,4 BIS[BIS(3 METHOXYCARBONYL 1 AZULENYL)METHYL]BENZENE; 1,4 PHENYLENEBIS[BIS(3 METHOXYCABONYL 1 AZULENYL)METHYLIUM]BIS(HEXAFLUOROPHOSPHATE); 2,5 BIS[BIS(3 METHOXYCARBONYL 1 AZULENYL)METHYLIDENE] 2,5 DIHYDROFURAN; 2,5 BIS[BIS(3 METHOXYCARBONYL 1 AZULENYL)METHYLIDENE] 2,5 DIHYDROTHIOPHENE; 2,5 FURYLENEBIS[BIS(3 METHOXYCARBONYL 1 AZULENYL)METHYLIUM]BIS(HEXAFLUOROPHOSPHATE); 2,5 THIENYLENEBIS[BIS(3 METHOXYCARBONYL 1 AZULENYL)METHYLIUM]BIS(HEXAFLUOROPHOSPHATE); 7,7,8,8 TETRAKIS(3 METHOXYCARBONYL 1 AZULENYL) 4 QUINODIMETHANE; ALDEHYDE DERIVATIVE; AZULENE DERIVATIVE; DICHLOROMETHANE; METHANE; METHYL 1 AZULENECARBOXYLATE; QUINODIMETHANE DERIVATIVE; TEREPHTHALALDEHYDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; ELECTROCHEMICAL ANALYSIS; OXIDATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; REDUCTION;

EID: 40649126899     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.02.012     Document Type: Article

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