Alkaloids of Stephania hernandifolia VI. Hernandifoline

Summary A new hasubanan alkaloid with the composition C₂₉H₃₃O₉N, mp 128–129°C₉ from ether), [] _D ²⁰ – 25° (c 2; ethanol) containing an ester group has been isolated from the herbStephania hernandifolia and has been called hernandifoline.All-Union Scientific-Research Institute for Medicinal Plants. Translated from Khimiya Prirodynkh Soedinenii, No. 2, pp. 158–164, March, 1971.     

Alkaloids of Fumaria vaillantii structure of vaillantine

Summary The plantFumaria vaillantii Loisl. has yielded protopine, fumaridine, fumaramine, d--hydrastine,l-adlumine, d-bicuculline, andl-adlumidine (this being the first time thatl-adlumidine has been isolated from the genusFumaria), and the new base vaillantine. On the basis of UV, IR, NMR, and mass spectra, and also the identity of O,O-dimethylvaillantine with muramine, the structure of vaillantine has been established as 2,3-didemethylmuramine.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 476–478, July–August, 1974.     

Withanolides of Physalis I. Physalactone

Summary 1. A new withanolide, which has been called physalactone, has been isolated fromPhysalis alkekengi L. growing in Turkmenia. It has the structure of 4,17,20(R)-trihydroxy-3-methoxy-1-oxo-5,6-epoxy-22R-witha-8(14), 24-dienolide.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 531–534, July–August, 1977.     

Pinusolide, a new diterpenoid from Pinus sibirica and P. korsensis

Conclusions From the neutral fraction of the oleoresin ofPinus sibirica R. Mayr andP. koraensis Sieb. et Zucc. a new diterpenoid has been isolated which we have called pinusolide, whose structure has been shown to be that of methyl labd-8(20)-1,3-dien-16,15-olid-19-oate.Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 541–545, September–October, 1970.     

Coumarin composition of the roots, stems, and fruit of Prangos lophoptera

Summary The coumarin composition of the roots, stems, and fruit ofPrangos lophoptera has been studied; in addition to known coumarin derivatives two new compounds have been isolated and have been calledisogosferol (XIII) andlophopterol (XIV).On the basis of a study of the IR, mass, and NMR spectra, and chemical properties of the latter, the most probable structure of 6-(3-hydroxy-1,2-ethoxyisopentyl)-7-methoxycoumarin has been proposed for it.Leningrad Sanitary-Hygienic Medical Institute. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 708–710, November–December, 1974.     

Isolation of the galactan ofPhyllophora nervosa and characterization of its structure

Summary 1. The chemical composition of the galactan of the Black-Sea algaPhyllophora nervosa has been established and its structure has been studied. The polysaccharide is linear and is constructed of D-galactose residued connected by 1 3 glycosidic bonds and of 3,6-anhydro-D-galactose residues connected by 1 4 bonds:-(4-0--D-Galp-13--D-3,6-AhGalp-1)-.2. The ester nature of the bond of the sulfuric acid residues with the primary and secondary carbon atoms of the galactose residues has been shown.M. V. Lomonosov Odessa Technological Institute of the Food Industry. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 693–698, November–December, 1976.     

Triterpene glycosides and their genins fromThalictrum foetidum. II. The structure of cyclofoetigenin A

A glycoside isolated from the epigeal parts ofThalictrum foetidum (Ranunculaceae) has yielded a new genin — cyclofoetigenin A, the structure of which has been established on the basis of chemical transformations and spectral characteristics as 24S-cycloartane-3,16,25,25-tetraol.Irkutsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 370–375, May–June, 1985.