Title of article
Syntheses of mono-, di- and triethynylazulenes
Author/Authors
Fabian، نويسنده , , Kai H.H and Elwahy، نويسنده , , Ahmed H.M and Hafner، نويسنده , , Klaus، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
4
From page
2855
To page
2858
Abstract
Simple and productive routes to mono-, di- and triethynylazulenes are described. Azulenes ethynylated in the five-membered ring can be prepared on a multigram scale by Pd-catalyzed cross-coupling of iodo- or bromoazulenes with trimethylsilyl-acetylene and subsequent desilylation. 5,7-Diethynylazulene was synthesized by dibromomethylenation of the corresponding dialdehyde and subsequent dehydrobromination.
Keywords
ethynylazulenes , Corey–Fuchs reaction , Pd-cross-coupling reaction
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1637072
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