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Updated: Nov 15, 2025

A Direct, Early Stage Guanidinylation Protocol for the Synthesis of Complex Aminoguanidine-containing Natural Products
Published on: September 9, 2016
C4-aldehyde of guaiazulene: synthesis and derivatisation
Georgia E Williams1, Gabriele Kociok-Köhn, Tony D James
1Department of Chemistry, University of Bath, Bath, BA2 7AY, UK. s.e.lewis@bath.ac.uk.
Abstract:
Guaiazulene is an alkyl-substituted azulene available from natural sources and is a much lower cost starting material for the synthesis of azulene derivatives than azulene itself. Here we report an approach for the selective functionalisation of guaiazulene which takes advantage of the acidity of the protons on the guaiazulene C4 methyl group. The aldehyde produced by this approach constitutes a building block for the construction of azulenes substituted on the seven-membered ring. Derivatives of this aldehyde synthesised by alkenylation, reduction and condensation are reported, and the halochromic properties of a subset of these derivatives have been studied.
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