The seed oils of some species of the family Cruciferae

Summary The physicochemical properties of the oils of the seeds of seven plants of the family Cruciferae —Cakile maritima, Sisymbrium altissimum, Sisymbrium Loeselii, Descurainia Sophia, Erysimum cheiranthoides, Brassica amoracioides andCrambe pontica — have been studied and their fatty acid compositions have been determined. The results obtained showed no marked differences from those given in the literature.Zaporozhe Medical Institute. Ukrainian Scientific-Research Institute of the Oils and Fats Industry. Zaporozhe Oils and Fats Combine. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 15–18, January–February, 1973.     

The polybuffer separation of the alkaloids of Vinca erecta

Summary By separating the total alkaloids ofV.erecta according to their basicities in an APS, in addition to bases known previously we have isolated ervincidine, apovincamine, (+)-quebrachamine, dl-eburnamine, (–)-1,2-dehydroaspidospermidine, and kopsanone. This is the first time that these alkaloids have been obtained from this plant. Thin-layer chromatography showed the presence of another 10–12 uncharacterized alkaloids.The region of the passage into the buffer solutions of some alkaloids has also been established.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 713–717, November–December, 1970.     

Amounts of arachidonic acid in the buds of Populus balzamifera in the course of the annual cycle

The paper gives information on the amount of arachidonic acid in the buds ofPopulus balzamifera. The presence of arachidonic acid in the buds was confirmed by TLC, GLC, coulometric titration, and an iodine number calculation. The dynamics of the amount of arachidonic acid in the buds during the annual cycle are given.Siberian Branch of the Technological Institute, Krasnoyarsk. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 513–516, July–August, 1987.     

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.     

Characteristics of the water-soluble polysaccharides of the leaves ofSilphium perfoliatum

The characteristics of the water-soluble complex of the leaves ofSilphium perfoliatum are given. The presence in them of acidic components of the type of pectic substances containing considerable amounts of compounds of protein nature has been shown. It has proved to be possible to separate the latter from the carbohydrate component by fractionation on DEAE-cellulose.M. V. Lomonosov Odessa Technological Institute of the Food Industry. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 771–774, November–December, 1979.     

Polysaccharides of Eremurus. XXVI. Study of the structure of the pectin from the leaves of Eremurus regelii

The partial acid hydrolysis of the homogeneous fraction C of the pectin fromEremurus regelii Vved. leaves has given a galacturonan. Its structure has been established on the basis of the results of periodate-nitric acid oxidation, methylation, and¹³C NMR spectroscopy.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 191–194, March–April, 1993.     

Esters of Ferula karakalensis. Structure and stereochemistry of karaferin and karaferinin

Two new guaiane esters — karaferin and karaferinin — have been isolated fromFerula karakalensis, and their structures and stereochemistry have been established. It has been shown that theFerula sesquiterpene alcohols angrendiol, ugamdiol, and karaferol are biogenetically interconnected and are products of a single chain of the biogenesis of terpenoids in plants.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent; Botanical Garden of Moscow State University. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 227–231, March–April, 1993.     

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.     

Isoprenoids of various species of the genus Betula

The review contains an analysis of the literature up to 1986, inclusive on the chemical investigation of some species of the genusBetula (family Betulaceae). Attention is devoted mainly to the distribution of the triterpene compounds in various parts of birch trees, and their biological properties and prospects are also discussed. Information (structure, melting point, angle of rotation, source) is given on 33 triterpenoids of the dammarane series isolated from the leaves, catkins, and young twigs of birch trees, and of 23 triterpenoids of the lupane and -amyrin series isolated from the outer bark.Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, USSR Academy of Sciences, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 325–341, May–June, 1988.     

Phospholipids of the seeds of two species of Erysimum

Summary The phospholipid complexes of the seeds ofErysimum diffusum andE. sylvestris have been investigated. It has been found that the amount of phospholipids in the seeds ofE. diffusum is lower than in those ofE. sylvestris, but their qualitative compositions are similar. The fatty-acid compositions of the triglycerides and of the total phospholipids of the two plants investigated have been studied. It has been established that the total phospholipids of the species ofErysimum under consideration and individual fractions of them differ by the degree of saturation and the qualitative and quantitative composition of the acids that they contain and, consequently, the phospholipids present in greatest amount differ in their molecular compositions.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 623–627, September–October, 1977.     

Alkaloids ofVeratrum,Petilium, andKorolkowia

The review is devoted to a study of the steroid alkaloids of plants of the generaVeratrum, Petilium, andKorolkowia. Characteristic reactions, spectra, and some chemical transformations of the alkaloids subdivided into groups according to structure are discussed. Some methods for determining their structures are considered.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 3–22, January–February, 1980.     

Umbrofine and 6-acetylumbrofine — New C18-diterpene alkaloids from Aconitum umbrosum

Two new alkaloids — umbrofine and 6-acetylumbrofine — have been isolated fromAconitum umbrosum, and their structures have been established on the basis of spectral characteristics.Institute of Chemistry of Plant Substances, Uzbekistan Republic Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedenini, No. 1, pp. 73–77, January–February, 1993.     

Histones of the cotton plant. Molecular characteristics of histone H1

A characterization of the histones of two varieties of the cotton plant,Gossypium hirsutum andG. barbadense, has been given with the aid of various electrophoretic systems. Their molecular weights have been determined. An analysis has been made of the cleavage of histone H1 at tyrosine residues. The positive charge and the molecular length of histone H1 have been determined by the method of incomplete succinylation.V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tadzhik SSR, Dushanbe. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 491–497, July–August, 1986.     

The structure of arnifolin

Summary Structure (I) is proposed for arnifolin — a sesquiterpene lactone fromArnica foliosa Nutt. andArnica montana L.All-Union Scientific-Research Institute for Medicinal Plants. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 270–272, May–June, 1971.     

Phospholipids of Gossypium barbadense

Summary From the total phospholipids of the cotton plant of the thin-fibered variety 5904-I(Gossypium barbadense) chromatographically homogeneous fractions of phosphatidylethanolamines, phosphatidylcholines, and phosphatidylinositols have been isolated. The well-known glycerophospholipid structure of these fractions has been established on the basis of their IR spectra and the products of their acid hydrolysis.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 558–560, September–October, 1974.     

Applications of1H and13C NMR spectroscopy in structural investigations of Vinca indole alkaloids

This review considers the laws connecting the parameters of the¹H and¹³C NMR spectra with the structure of the substances and the use of these laws for solving structural and stereochemical problems of theVinca indole alkaloids and other compounds of closely related structure. For each type of alkaloids, characteristic features of the PMR and¹³C NMR spectra are given that permit the structures of similar bases to be established and their stereochemical identification to be performed.Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 3–15, January–February, 1986.     

Use of the paramagnetic shift agent Eu(DPM)3 for studying the structure and stereochemistry of conferol and conferone

Summary A spectrophotometric method is proposed for determining the content of aspidin in a crystalline powder and in the rhizomes of the fernsDryopteris spinulosa (M),D. phegopteris (L.), andD. fragrans (L.) Schott.All-Union Scientific-Research Institute for Medicinal Plants. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 684–687, November–December, 1970.     

Insect pheromones and their analogs. XLVII. Synthesis of 11-oxododeca-3,6-diynoic acid — The acyclic precursor of a macrolide component of pheromones of Oryzaephilus mercator and O. Surinamensis

A new approach is proposed to the synthesis of 11-oxododeca-3,6-diynoic acid — the acyclic precursor of a macrolide component of pheromones ofOryzaephilus mercator andO. surinamensis — from the readily available tetrahydropyran or allylacetone via the intermediate 5-bromo-2,2-ethylenedioxypentane.Institute of Organic Chemistry, Urals Division, Russian Academy of Sciences, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 2, pp. 288–292, March–April, 1993.     

Phytoecdysteroids of plants of the genus Silene. XVII. Ecdysterone 22,25-di-O-benzoate from Silene scabrifolia

The new phytoecdysteroid ecdysterone 22,25-di-O-benzoate (IV) has been isolated from the epigeal organs ofSilene scabrifolia Kom. The alkaline hydrolysis of (IV) gave ecdysterone 25-O-benzoate and ecdysterone (I). Details of the IR, UV, mass, PMR, and¹³C NMR spectra of compound (IV) are given.Institute of the Chemistry of Plant Substances, Uzbek SSR Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 363–366, May–June, 1990.