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The reaction of 1,2-naphthoquinone 1-methides with syncarpic acid

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Chemistry of Heterocyclic Compounds Aims and scope

The reaction of syncarpic acid with Mannich bases derived from 2-naphthol yielded 8,12-dihydro-9H-benzo[a]xanthene-9,11(10H)-diones as products of the Diels–Alder reaction with inverse electron demands involving 1,2-naphthoquinone 1-methides generated in situ and dehydration.

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This work was supported by the Russian Foundation for Basic Research (project No. 17-03-01158) and the Ministry of Education and Science of the Russian Federation within the framework of the baseline of the State assignment for scientific activity (No. 4.6764.2017/BCh)

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  1. Samara State Technical University, 244 Molodogvardeyskaya St, Samara, 443100, Russia

    Anton V. Lukashenko, Dmitry V. Osipov, Vitaly А. Osyanin & Yuri N. Klimochkin

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  1. Anton V. Lukashenko
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  2. Dmitry V. Osipov
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  3. Vitaly А. Osyanin
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  4. Yuri N. Klimochkin
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2019, 55(10), 1004–1006

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Lukashenko, A.V., Osipov, D.V., Osyanin, V.А. et al. The reaction of 1,2-naphthoquinone 1-methides with syncarpic acid. Chem Heterocycl Comp 55, 1004–1006 (2019). https://doi.org/10.1007/s10593-019-02569-4

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  • DOI: https://doi.org/10.1007/s10593-019-02569-4

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