Junya Higashi

Synthesis of Redox‐Active, Intramolecular Charge‐Transfer Chromophores by the [2+2] Cycloaddition of Ethynylated 2<i>H</i>‐Cyclohepta[<i>b</i>]furan‐2‐ones with Tetracyanoethylene

Taku Shoji, Junya Higashi, Shunji Ito et al. · Chemistry - A European Journal · 2011 · 62 citations

Synthesis and Redox Behavior of 1‐Azulenyl Sulfides and Efficient Synthesis of 1,1′‐Biazulenes

Taku Shoji, Junya Higashi, Shunji Ito et al. · European Journal of Organic Chemistry · 2008 · 50 citations

Chemical Engineering, Derivatives, Redox Behavior +10

Synthesis of donor–acceptor chromophores by the [2 + 2] cycloaddition of arylethynyl-2H-cyclohepta[b]furan-2-ones with 7,7,8,8-tetracyanoquinodimethane

Taku Shoji, Junya Higashi, Shunji Ito et al. · Organic & Biomolecular Chemistry · 2012 · 39 citations

Organic Charge-transfer Compound, Chemical Engineering, Engineering +13

Electrophilic <i>ipso</i>‐Substitution and Some Unique Reaction Behavior of 1,3,6‐Tri‐<i>tert</i>‐butylazulene

Taku Shoji, Shunji Ito, Tetsuo Okujima et al. · European Journal of Organic Chemistry · 2009 · 32 citations

Chemical Engineering, Engineering, Organic Electrochemistry +9

Heteroarylation of 1‐Azulenyl Methyl Sulfide: Two‐Step Synthetic Strategy for 1‐Methylthio‐3‐(heteroaryl)azulenes Using the Triflate of <i>N</i>‐Containing Heterocycles

Junya Higashi, Taku Shoji, Shunji Ito et al. · European Journal of Organic Chemistry · 2008 · 26 citations

Chemical Engineering, Derivatives, Redox Behavior +10