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Synthetic approaches towards bisspiro[naphthalene-2(1H),3′-(3H)pyrazol]-1-one-containing compounds

  • A. Girgis EMAIL logo , F. Osman , F. El-Samahy and I. Ahmed-Farag
Published/Copyright: June 1, 2006
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Abstract

1,3-Dipolar cycloaddition reaction of bis{[4-(3,4-dihydro-(2H)-naphthalen-1-oxo-2-yl)methyl-idenephenyl]oxy}alkanes with nitrilimines (generated in situ by triethylamine dehydrohalogenation of the corresponding hydrazonoyl chlorides) in refluxing dry benzene afforded a mixture of monocycloadduct and dicycloadduct products in high regioselectivity. On the other hand, reaction of bis{[2-(3,4-dihydro-(2H)-naphthalen-1-oxo-2-yl)methylidenephenyl]oxy}alkanes with nitrilimines gave the corresponding dicycloadducts as the only isolable regioisomers.

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Published Online: 2006-6-1
Published in Print: 2006-6-1

© 2006 Institute of Chemistry, Slovak Academy of Sciences

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