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Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine

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Chemistry of Natural Compounds Aims and scope

Novel berberine derivatives with annelated four-membered sulfone rings were synthesized. Cycloaddition of alkanesulfonyl chlorides to dihydroberberine occurred with high stereoselectivity and formed a single stereoisomer.

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Acknowledgment

We thank Khimiya Center for Common Use, SB, RAS, for making the spectral and analytical measurements.

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Authors and Affiliations

  1. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, 9 Prosp. Lavrent’eva, 630090, Novosibirsk, Russia

    E. D. Gladkova, O. A. Luzina & N. F. Salakhutdinov

  2. Novosibirsk State University, Pirogova St, 630090, Novosibirsk, Russia

    E. D. Gladkova

Authors
  1. E. D. Gladkova
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  2. O. A. Luzina
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  3. N. F. Salakhutdinov
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Corresponding author

Correspondence to E. D. Gladkova.

Additional information

Translated from Khimiya Prirodnykh Soedinenii, No. 6, November–December, 2021, pp. 910–912.

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Gladkova, E.D., Luzina, O.A. & Salakhutdinov, N.F. Stereoselective Cycloaddition of Alkanesulfonyl Chlorides to Dihydroberberine. Chem Nat Compd 57, 1062–1065 (2021). https://doi.org/10.1007/s10600-021-03550-4

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  • DOI: https://doi.org/10.1007/s10600-021-03550-4

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