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981.
G. P. Bakhaeva Yu. A. Berlin M. N. Kolosov O. A. Chuprunova 《Chemistry of Natural Compounds》1969,3(6):339-342
Summary It has been shown that olivomycose has the structure of 3-C-methyl-2, 6-dideoxy-L-arabino-hexose. In olivomycins A and C, this sugar is present in the form of the 4-O-isobutyrate, and in olivomycin B in the form of the 4-O-acetate.Khimiya Prirodnykh Soedinenii, Vol. 3, No. 6, pp. 405–410, 1967For preliminary communication, see [1]. 相似文献
982.
Summary For the primary alkyl halides (R=from C2H5 to n-C9H19; halogen=C1, Br, and I) and the simplest aryl halides (R=C6H5 and p-CH3C6H4) it was shown that the organomagnesium synthesis in absence of catalysts for the Grignard reaction can be applied with success to the preparation of heteroorganic compounds of elements of Groups II–IV (mercury, boron, aluminum, silicon, germanium, tin, phosphorus, arsenic, antimony). 相似文献
983.
Shahkel'dyan I. V. Melekhina E. K. Atroshchenko Yu. M. Efremov Yu. A. Alifanova E. N. Kopyshev M. V. Troitskii N. A. Subbotin V. A. Nikishina M. B. 《Russian Journal of Organic Chemistry》2003,39(4):589-595
A series of 7-carboxy-3-R-1,5-dinitro-3-azabicyclo[3.3.1]non-6-enes was synthesized by reduction of 3,5-dinitrobenzoic acid with sodium borohydride followed by Mannich reaction with formaldehyde and primary amines. The mechanism of decomposition under electron impact of the 3-azabicyclo[3.3.1]nonane was established. Enthalpies of formation of compounds synthesized were calculated by semiempirical PM3 method. 相似文献
984.
Shul'ga Yu. M. Chernushevich I. V. Dzhardimalieva G. I. Roshchupkina O. S. Dodonov A. F. Pomogailo A. D. 《Russian Chemical Bulletin》1994,43(6):983-987
Russian Chemical Bulletin - The monomer [Cr3O(OCOCH=CH2)6]OH was produced by reaction of acrylic acid with fresh chromium hydroxide. This monomer was investigated by a number of physicochemical... 相似文献
985.
A. V. Borovkov Yu. N. Brusil'tsev A. O. Doroshenko 《Theoretical and Experimental Chemistry》1993,28(4):269-273
An investigation was carried out of the spectral-luminescent and acid-base properties at the stage of formation of the hydrogen bond and during the protonation of compounds with annelated aromatic and heterocyclic rings, obtained by introduction of bridging groups -CH=CH- (I), -CH=N- (II) and -CO-N(CH3)-(III) in the 4- and 2-positions of the molecules of 4-substituted derivatives of 2,5-diphenyloxazole. The nature of the reaction center was estabished, and an analysis was carried out of its sensitivity to the electronic influence of the substituents, and the reasons for the observed differences in the properties of compounds of various reaction series are discussed. A comparative analysis of the fluorescent properties of the neutral and protonated forms of the oxazole derivatives studied was made and the conclusion that the generation is possible of laser emission by the protonated forms of compounds of the reaction series (I) was confirmed.Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 28, No. 4, pp. 343–349, July–August, 1992. 相似文献
986.
M. M. Krayushkin M. A. Kalik L. G. Vorontsova E. Yu. Zvezdina M. G. Kurella 《Russian Chemical Bulletin》1993,42(7):1204-1208
9-Methyl-3,3a,4,5-tetrahydro-6H-thieno[2,3-b]thiocino[4,5-c]isoxazole and 9-hydroxyimino-2-methyl-7-methylene-6, 7,8,9-tetrahydro-5H-thieno[2,3-b]thiocine have been prepared for the first time by the oxidation of 2--alkenylthio-3-thiophenecarbaldoximes with NaOCl. X-ray structural investigations of thieno[2,3-b]thiocine and 2-homomethallylthio-5-methyl-3-thiophenecarbaldoxime have been carried out.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1262–1266, July, 1993. 相似文献
987.
V. A. Pankratov Ts. M. Frenkel A. E. Shvorak S. V. Lindeman Yu. T. Struchkov 《Russian Chemical Bulletin》1993,42(1):81-87
A 11-complex of trinitrophenol with benzyldimethylamine (1) and a 111-complex, the product of the interaction of benzyldimethylamine, glycidyl phenyl ether, and phenol (2), have been synthesized and characterized by means of X-ray analysis. Complex1 is a precursor for the catalysts of selective isocyanate cyclotrimerization, while complex2 is one of those catalysts. In the crystal structure complex1 forms H-bonded cationic-anionic aggregates with proton transfer from phenol to the N-atom of the tertiary amine. Complex2 crystallizes as a monohydrate (2a) with a strong H-bond between the quaternary ammonium and phenolic components, and exists in crystals in the form of globular H-bonded dimeric hydrates. Possible pathways of dissociation of complex2a are discussed. The data obtained may be used as a basis for further interpretation of the regularities of cyclotrimerization of isocyanates catalyzed by complexes of this type.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No 1, pp. 92–97, January, 1993. 相似文献
988.
989.
990.
I. A. Ronova L. V. Dubrovina A. Yu. Kovalevskii C. Hamciuc M. Bruma 《Russian Chemical Bulletin》1998,47(7):1248-1256
Hindered rotation was considered in calculations of the conformational parameters of a series of polyheteroarylenes with bulky
side substituents by the Monte-Carlo method. Within the range of experimental errors, the results of calculations for several
polyarylates coincide with the values of conformational rigidity, determined from hydrodynamic experimental data. The proposed
procedure was used to estimate the rigidities of a number of polymers with bulky side substuents for which experimental determination
is difficult.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1287–1296, July, 1998. 相似文献