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Synthesis of 3-methyl-3,4-dihydroisoquinolines based on myristicin

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Abstract

The reaction of a natural allylbenzene, myristicin, with nitriles afforded a series of 7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline and 6,7-dihydro[1,3]dioxolo[4,5-h]isoquinoline derivatives.

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References

  1. Mashkovskii, M.D., Lekarstvennye sredstva (Drugs), Moscow: Meditsina, 1993, vol. 1, p. 628.

    Google Scholar 

  2. Mashkovskii, M.D., Lekarstvennye sredstva (Drugs), Moscow: Meditsina, 1993, vol. 1, p. 183.

    Google Scholar 

  3. Kornienko, A. and Evidente, A., Chem. Rev., 2008, vol. 108, p. 1982.

    Article  CAS  Google Scholar 

  4. Bischler, A. and Napieralski, B., Ber., 1893, vol. 26, p. 1903.

    Article  Google Scholar 

  5. Shklyaev, Yu.V., Smolyak, A.A., and Gorbunov, A.A., Russ. J. Org. Chem., 2011, vol. 47, p. 239.

    Article  CAS  Google Scholar 

  6. Shklyaev, Yu.V., Smolyak, A.A., Firgang, S.I., and Konyushkin, L.D., Russ. Chem. Bull., Int. Ed., 2012, vol. 61, p. 1627.

    Article  CAS  Google Scholar 

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Correspondence to A. A. Smolyak.

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Original Russian Text © A.A. Smolyak, L.D. Konyushkin, S.I. Firgang, Yu.V. Shklyaev, 2016, published in Zhurnal Organicheskoi Khimii, 2016, Vol. 52, No. 12, pp. 1820–1823.

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Smolyak, A.A., Konyushkin, L.D., Firgang, S.I. et al. Synthesis of 3-methyl-3,4-dihydroisoquinolines based on myristicin. Russ J Org Chem 52, 1812–1816 (2016). https://doi.org/10.1134/S1070428016120174

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  • DOI: https://doi.org/10.1134/S1070428016120174

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