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Bortolini, O., D’Agostino, M., De Nino, A., Maiuolo, L., Nardi, M. and Sindona, G. (2008) Solvent-free, microwave assisted 1,3-cycloaddition of nitrones with vinyl nucleobases for the synthesis of N,O-nucleosides, Tetrahedron, 64, 8078-8081. doi:10.1016/j.tet.2008.06.074

has been cited by the following article:

• TITLE: Reactivity of 1-methylisoquinoline synthesis of pyrazolyl triazoloisoquinoline and thia-diazolyl isoquinoline derivatives

  AUTHORS: Hamdi M Hassaneen, Huwaida M. E Hassaneen, Yasmin Sh Mohammed

  KEYWORDS: [1, 2, 4]Triazolo[3, 4-a]isoquinolines; Enaminones; Hydrazonoyl Halides; Cycloaddition Reactions; Chitosan; Thioanilides; [1, 3, 4]Thiadiazolylisoquinoline Derivatives

  JOURNAL NAME: Natural Science, Vol.3 No.8, August 3, 2011

  ABSTRACT: The reaction of 1-methylisoquinoline 1 with hy-drazonoyl halides 2 in ethanol in the presence of chitosan under microwave irradiation affords triazoloisoquinoline 4. Product 4 reacts with dimethylformamide-dimethylacetal to give ena- minones 7 which react with hydrazonoyl halides to give pyrazolyl triazoloisoquinoline 13. Also, 1-methylisoquinoline 1 reacts with arylisothio-cyanate to give thioanilide 15 which reacts with hydrazonoyl halides to give the corresponding thiadiazolyl isoquinoline derivatives 20, 24.