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The structure of ulopterol

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Chemistry of Natural Compounds Aims and scope

Conclusions

A new coumarin C15H18O5 with mp 141.5–142.5° C (from benzene) has been isolated from the roots and fruit ofPrangos uloptera D. C., and it has been called “ulopterol.” On the basis of UV, IR, NMR, and mass spectra it has been found to have the structure of 6-(2′,3′-dihydroxy-3′-methylbutyl)-7-methoxy-coumarin and is a geometrical isomer of meranzin hydrate.

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References

  1. A. Z. Abyshev and A. M. Kutnevich, KhPS [Chemistry of Natural Compounds], 4, 378, 1968.

    CAS  Google Scholar 

  2. Yu. N. Sheinker, G. Yu. Pek, and M. E. Perel'son, DAN, 158, 1382, 1964.

    CAS  Google Scholar 

  3. G. A. Kuznetsova, Natural Coumarins and Furocoumarins [in Russian], 1967.

  4. G. A. Kuznetsova and A. Z. Abyshev, KhPS [Chemistry of Natural Compounds], 1, 283, 1965.

    Article  Google Scholar 

  5. K. Hata, M. Kozawa, Y. Ikeshiro, and K.-Y. Yen, J. Pharm. Soc. Japan, 88, no. 5, 513, 1968.

    Article  CAS  Google Scholar 

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Khimiya Prirodnykh Soedinenii, Vol. 6, No. 3, pp. 300–304, 1970

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Abyshev, A.Z., Kutnevich, A.M., Kostyuchenko, N.P. et al. The structure of ulopterol. Chem Nat Compd 6, 301–303 (1970). https://doi.org/10.1007/BF00567304

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  • DOI: https://doi.org/10.1007/BF00567304

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