Zeravshanisine — A new alkaloid from Aconitum zeravschanicum

The new diterpene alkaloid zeravshanisine has been isolated from the epigeal part ofAconitum zeravschanicum Steinb.. Its structure has been established by spectral methods and by x-ray structural analysis as 2-acetyl-13-benzoyl-14-hydroxyhetisine.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Institute of Organometallic Compounds, Russian Academy of Sciences, Moscow. Translated from Khimiya Prirodnykh Soedinenii, Nos. 3,4, pp. 375–382, May–August, 1992.     

New derivatives of (?)-neocembrene from the soft coral Sarcophyton trocheliophorum

A hexane extract of the soft coralSarcophyton trocheliophorum has yielded two new diterpenoids for which the structures of 13S-hydroxy-(–)-neocembrene and 13S-hydroxy-11,12-epoxy-(–)-neocembrene have been established.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 535–540, July–August, 1988.     

Alkaloids of the cultivated species Aconitum tauricum

Mesaconitine, hypaconitine, and the new alkaloid taurenine have been isolated from the roots of the cultivated speciesAconitum tauricum, and the structure of taurenine has been established.Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences. Polar-Alpine Botanical Garden, Kola Branch, Russian Academy of Sciences, Apatity. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 108–112, January–February, 1992.     

Structure of stachysolone

Summary It has been shown that stachysolone — a bitter substance fromStachys annua L. — is a diterpenoid with a rearranged labdane hydrocarbon skeleton of the kolavane type. Structural formula (I) has been established for stachysoloneInstitute of Chemistry, Academy of Sciences of the Moldavian SSR. Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czechoslovakian SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 295–299, May–June, 1972.     

Crystal and molecular structure of the sesquiterpene humulane ester juniferdin

The spatial structure of the sesquiterpene humulane ester juniferdin, isolated fromFerula juniperina, has been established by the x-ray structural method. An analysis is given of the 11-membered humulane ring in comparison with the conformation observed in fexerol and juniferol.Institute of Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Institute of Crystallography, Academy of Sciences of the USSR, Moscow. Translated from Khimiya Prirodnykh Soedinii, No. 4, pp. 494–499, July–August, 1991.     

Lipids of the biomass ofRuta graveolens, grownin vivo andin vitro

A lower content of chlorophylls, phospholipids, and linolenic acid and a higher content of rutin, carotenoids, and xanthophylls in the biomass ofRuta graveolens L. obtainedin vitro has been found as compared with these indices from the epigeal part of the plant grownin vivo.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent. Institute of Botany, Academy of Sciences of the Republic of Uzbekistan, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 651–655, September–October, 1993.     

Phytoecdysteroids of plants of the genus Serratula. Ajugasterone C 20,22-monoacetonide from Serratura wolffii

The phytoectysteroids of the epigeal part of the plantSerratula wolffii Andrae have been investigated. The structure of a new ecdysteroid — ajugasterone C 20,22-monoacetonide has been established. Seven known acdysteroids have been isolated and identified.Institute of Biochemistry, Ukrainian Academy of Sciences, Kiev. Institute of Plant Substances, Uzbekistan Republic Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 71–76, January–February, 1992.     

Coumarins of Fraxinus mandschurica and F. potamophila

Summary The leaves ofFraxinus mandschurica Rupr. and the bark ofF. potamophila Herd. have yielded esculetin, fraxinol, and a new coumarin C₁₀H₈O₅, mp 228–230°C which we have called isofraxetin. On the basis of NMR and UV spectroscopy it has been established that isofraxetin is 5,7-dihydroxy-7-methoxycoumarin.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Institute of Chemistry, Academy of Sciences of the Turkmen SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 493–497, July–August, 1973.     

Compounds of the pyran series as components of the essential oils ofTanacetum boreale andAjania fastigiata

It has been established that the essential oils ofTanacetum boreale andAjania fastigiata contain as their main components 3-hydroxy-2,2,6-trimethyl-6-vinyltetrahydropyran and its acylated and oxidized derivatives.Institute of Chemical Sciences, Academy of Sciences of the Kazakh SSR, Alma-Ata. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 332–335, May–June, 1985.