A new coumarin — Obtusifol from Haplophyllum obtusifolium

May 1974, Volume 10, Issue 3, pp 311–315 | Cite as

Article

First Online: 01 May 1974

Received: 15 February 1973

Conclusions

A new coumarin obtusifol, C₁₅H₁₆O₆, with mp 149.5–150°C has been isolated fromHaplophyllum obtusifolium for the first time.

The structure of 2′- or 3′-(1-hydroxy-1-methylethyl)-8-methoxy[1,4]dioxano[g]coumarin has been proposed for obtusifol.

It has been shown that the genusHaplophyllum is close in respect of its coumarin composition to the genusPtaeroxylon.

Coumarin Ferric Chloride Singlet Signal Esculetin Hydrobromic Acid

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1.
G. A. Kuznetsova and N. F. Gashimov, Abstracts of Lectures at an International Symposium on “The Chemistry of the Natural Compounds of the Balkan Flora,” Bulgaria (1971), p. A22.Google Scholar
2.
G. A. Kuznetsova and N. F. Gashimov, Khim. Prirodn. Soedin., 666 (1972).Google Scholar
3.
G. A. Kuznetsova and N. F. Gashimov, Khim. Prirodn. Soedin., 113 (1973).Google Scholar
4.
G. A. Kuznetsova in: Natural Coumarins and Furocoumarins [in Russian], Leningrad (1967), p. 81.Google Scholar
5.
F. M. Dean, and D. A. H. Taylor, J. Chem. Soc., (C), 114 (1966).Google Scholar
6.
F. M. Dean and B. Parton, J. Chem. Soc. (C), 526 (1969).Google Scholar
7.
E. Spath, and Z. Jermanowska, Ber.70, 698 (1937).Google Scholar

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