100677-63-2Relevant articles and documents
1,4,5,6-Tetrahydropyridazines by Cycloaddition of Enol Ethers to Azoalkenes and their Aromatisation to Pyridazines.
Clarke, Simon J.,Gilchrist, Thomas L.
, p. 3371 - 3389 (2007/10/02)
Transient azoalkenes generated from acyl- and 4-tolylsulphonyl-hydrazones of α-haloacetophenones and of ethyl bromopyruvate are intercepted by cycloaddition to enol ethers, giving 6-alkoxy-1,4,5,6-tetrahydropyridazines (2). 6-Alkoxy-3-aryl-1,4,5,6-tetrahydropyridazines are converted by reaction with sodium ethoxide into 3-arylpyridazines (3).