Title of article
From 1,4-diketones to N-vinyl derivatives of 3,3′-bipyrroles and 4,8-dihydropyrrolo[2,3-f]indole in just two preparative steps
Author/Authors
Trofimov، نويسنده , , Boris A. and Zaitsev، نويسنده , , Alexey B. and Schmidt، نويسنده , , Elena Yu. and Vasilʹtsov، نويسنده , , Alexander M. and Mikhaleva، نويسنده , , Alʹbina I. and Ushakov، نويسنده , , Igorʹ A. and Vashchenko، نويسنده , , Alexander V. and Zorina، نويسنده , , Nadezhda V.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
3
From page
3789
To page
3791
Abstract
Dioximes of hexane-2,5-dione and cyclohexane-1,4-dione react with acetylene in an autoclave (KOH/DMSO, 100 °C, 1 h, initial pressure 14 atm) to give 2,2′-dimethyl-1,1′-divinyl-[3,3′]bipyrrole and 1,5-divinyl-4,8-dihydropyrrolo[2,3-f]indole in 12% and 6% yields, respectively, thus exemplifying a very simple, straightforward route to inaccessible or unknown pyrrolic assemblies.
Keywords
3 , 3?-Bipyrroles , Pyrroloindoles , Dioximes , Acetylene , Superbases
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1841544
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