Title of article
Synthesis of 1-(pyridyl, quinolyl, and isoquinolyl)azulenes by Reissert–Henze type reaction
Author/Authors
Shoji، نويسنده , , Taku and Okada، نويسنده , , Kazuyuki and Ito، نويسنده , , Shunji and Toyota، نويسنده , , Kozo and Morita، نويسنده , , Noboru، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
4
From page
5127
To page
5130
Abstract
Azulene derivatives reacted with N-oxide of several heterocycles in the presence of trifluoromethanesulfonic anhydride (Tf2O) to afford 1-(pyridyl, quinolyl, and isoquinolyl)azulenes in good yield, respectively. In the case of the reaction with the 1-azulenyl methyl sulfide (12), 1,1′-biazulene derivative 13 was obtained under the similar reaction conditions. The first synthesis of unsymmetrical 1,3-di(pyridyl)azulene derivative was also established via our new preparation method following the electrophilic pyridinylation using the reaction with pyridine in the presence of Tf2O.
Keywords
Azulene , Electrophilic arylation , heterocycle
Journal title
Tetrahedron Letters
Serial Year
2010
Journal title
Tetrahedron Letters
Record number
1874742
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