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1,3-Dipolar cycloaddition of phthalazinium ylides to 5-arylidene-2-spirocyclohexane-1,3-dioxane-4,6-diones

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Abstract

Tetrahydrospiropyrrolo[2,1-a]phthalazines were synthesized by the reaction of 5-arylidene-2-spirocyclohexane-1,3-dioxane-4,6-diones with phthalazinium ylides. One of the reaction products, viz., 3-ethoxycarbonyl-2-(4-methoxyphenyl)-2′,2′-pentamethylene-1,2,3,10b-tetrahydrospiro[pyrrolo[2,1-a]phthalazine-1,5′-[1,3]dioxane]-4′,6′-dione, was studied by X-ray diffraction. The spectroscopic characteristics of the reaction products are discussed.

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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 10, pp. 2362–2365, October, 2005.

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Sukhotin, A.V., Kartsev, V.G., Aleksandrov, Y.A. et al. 1,3-Dipolar cycloaddition of phthalazinium ylides to 5-arylidene-2-spirocyclohexane-1,3-dioxane-4,6-diones. Russ Chem Bull 54, 2437–2440 (2005). https://doi.org/10.1007/s11172-006-0134-1

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  • DOI: https://doi.org/10.1007/s11172-006-0134-1

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