A chemical study of plants of the Mongolian flora the flavonoids of two species of Oxytropis

Institute of Chemistry, Mongolian Academy of Sciences, Ulan-Bator. Institute of the Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 722–723, November–December, 1992.     

Construction of crystal structure sections using the clat software package

Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Institute of Physical Chemistry, Polish Academy of Sciences. Translated fromZhurnal Struktumoi Khimii, Vol. 36, No. 5, pp. 956–959, September–October, 1995.     

Triterpene glycosides of Scabiosa soongorica. V. β-Sitosterol β-D-glucopyranoside and songoroside A

Institute of Organic Chemistry, Academy of Sciences of the Kirgiz SSR, Frunze. Institute of the Chemistry of Plant Substances, Academy of Sciences of the Uzbek SSR, Tashkent. Translated from Khimiya Prirodynkh Soedinenii, No. 6, pp. 885–886, November–December, 1988.     

Production of (+)-norsolanadione

Institute of Chemistry, Bashkir Scientific Center, Urals Branch, Russian Academy of Sciences, Ufa. Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Novosibirsk. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 735–736, September–October, 1991.     

Refinement of the crystal and molecular structure of 4-phenylthiosemicarbazide diacetic acid monohydrate

Institute of Applied Physics, Academy of Sciences, Moldova Republic. Institute of Chemistry, Academy of Sciences, Moldova Republic. Translated fromZhurnal Strukturnoi Khimii, Vol. 35, No. 3, pp. 154–158, May–June, 1994.     

Coordinated diaminoguanidinium(1+) ion in the crystal structure of the [Cu(CH8N5)Cl3] complex

Institute of Inorganic Chemistry, Siberian Branch, Russian Academy of Sciences. Institute of Organoelement Compounds, Russian Academy of Sciences. Translated fromZhurnal Strukturnoi Khimii, Vol. 36, No. 5, pp. 936–941, September–October, 1995.     

Molecular structure of 10,10-dimethyl-7H-pyrano[4′,3′:4,5]thieno[3,2-e]-(1,2,4)-triazolo[2,3-e]pyrimidine

Institute of Fine Organic Chemistry, Armenian Academy of Sciences. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences. Translated fromZhurnal Strukturnoi Khimii, Vol. 35, No. 5, pp. 197–199, September–October, 1994.     

Influence of the temperature of cultivation on the lipid composition of the bacterium Yersinia pseudotuberculosis

Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, Academy of Sciences of the USSR, Vladivostok. Institute of Marine Biology, Far Eastern Branch, Academy of Sciences of the USSR, Vladivostok. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 579–580, July–August, 1991.     

Crystal and molecular structure of 1-(2′-methoxyphenyl)-3,7,10-trimethylstannatrane

A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences. Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated fromZhurnal Strukturnoi Khimii, Vol. 35, No. 5, pp. 199–203, September–October, 1994.     

Crystal and molecular structures of methyl (2-hydroxy-3-oxo-5-p-tolyl-2,3-dihydrofuran-2-yl)acetate

Institute of Chemical Physics in Chernogolovka, Russian Academy of Sciences. Institute of Technical Chemistry, Russian Academy of Sciences. A. M. Gorkii Perm State University. Translated fromZhurnal Struktumoi Khimii, Vol. 36, No. 5, pp. 952–956, September–October, 1995.     

Berberis alkaloids XIV. Dynamics of the accumulation of alkaloids in Berberis oblonga

Andizhan State Medical Institute. Institute of Chemistry of Plant Substances, Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 597–598, September–October, 1992.     

Essential oil of Artemisia rubripes

Tomsk State Medical Institute. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 859–860, November–December, 1991.     

Principal relationships of the heterogeneous catalytic oxidation of benzene and its derivatives

The results of investigations into the processes involved in the heterogeneous catalytic oxidation of benzene and its derivatives at the L. V. Pisarzhevskii Institute of Physical Chemistry, National Academy of Sciences of Ukraine, are summarized. The mechanisms of the full and partial oxidation of benzene, toluene, and their halogen derivatives are discussed. L. V. Pisarzhevskii Institute of Physical Chemistry, National Academy of Sciences of Ukraine, Kiev. Translated from Teoreticheskaya i éksperimental’naya Khimiya, Vol. 34, No. 3, pp. 133–147, May–June, 1998.     

Alkaloids of Aconitum orientale

Institute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent. Pyatigorsk Pharmaceutical Institute. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 864–865, November–December, 1991.     

Glycosylation of cyclosieversiosides A and H

Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan. Tashkent Pharmaceutical Institute. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 621–622, July–August, 1993.     

Composition of the essential oil of Thymus krylovii

Tomsk State Medical Institute. Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR. Translated from Khimiya Prirodynkh Soedinenii, No. 6, pp. 886–887, November–December, 1988.     

Conformational features of peptide fragments of the C-end of histone H1

The conformational possibilities of four synthesized oligopeptides with the amino acid sequences 165–172, 173–184, 152–172, and 152–184 of the C-end of histone H1 of calf thymus above been studied in solution under various conditions by the method of circular dichroism. V. I. Nikitin Institute of Chemistry, Academy of Sciences of the Tadchik SSR, Dushanbe. Institute of Cytology, Academy of Sciences of the USSR, Leningrad. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 793–798, November–December, 1990.     

Cyclization and rearrangements of diterpenoids

Institute of Chemistry, Moldavian Academy of Sciences, Kishinev. Translated from Khimiya Prirodnykh Soedinenii, No. 5, pp. 726–728, September–October, 1991.     

Structure of antigenic determinants of neurotoxin II from cobra venom

Institute of Biorganic Chemistry, Academy of Sciences of the Uzbek SSR. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 607–608, July–August, 1988.     

A chemical investigation ofMatteuccia struthiopteris

Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 608–609, July–August, 1993.