Crystal structure of the oxime of 2-acetylpyridine

Institute of Chemical Physics, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 3, pp. 113–115, May–June, 1991.     

Synthesis and nitration of 4,6(4,8)-dimethyl-4-methyl-6(8)-methoxy-1,2,3,4-tetrahydrospiro [quinoline-2-cyclohexanes]

The cydization of 1-allyl-1-arylaminocyclohexanes under conditions of acid catalysis afforded 1,2,3,4-tetrahydro-4-methylspiro [quinoline-2-cyclohexanes] methyl (methoxy)-substituted in the phenylene ring. Their mono- and dinitro derivatives were synthesized, and their structure was established. Propositions on the direction of the nitration reaction of these heterocyclic compounds were expressed.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 784–788, June, 1993.     

Anodic oxidation of olefins in presence of fluorine anion

Russian Chemical Bulletin -     

Synthesis of 3,6-dialkyl-4,5-dihydro-4,5-dichloro-2,1-benzisoxazoles from o-nitrophenylcyclopropanes

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 130–131, January, 1992.     

Synthesis and nitration of NH- and N-vinyl-4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines

It has been shown that the most efficient catalysts for the synthesis of 4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine from 1,2,5-trimethylpyridin-4-one and acetylene under Trofimov conditions are rubidium and potassium hydroxides. Use of Triton B or a mixture of trimethylbenzylammonium chloride with rubidium hydroxide as catalyst gives O-alkylated oxime. Their configurations and conformations were established through separation of the individual isomers of 1-vinyl-4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridines. Acetyl nitrate nitration of the cis isomer of this compound gave the 2- and 3-nitro derivatives. Similar nitration of 4,5,7-trimethyl-4,5,6,7-tetrahydropyrrolo[3,2-c]pyridine gave the 2-nitro-7-hydroxy derivative.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1375–1380, October, 1991.     

Direct generation of photons in\tilde v_e e-annihilation into hadrons

In the quark-parton model we obtain an expression for the effective cross section of the process of direct photon generation in the annihilation of an antineutrino and an electron into hadrons (_e + e + X). The angular and energy dependences of the photons are investigated. It is shown that for large photon energies, the contribution from hadronic radiation dominates that from leptonic radiation.Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 11, pp. 98–103, November, 1987.     

Investigation of the structure of 1,2-dihydro-3-(2-hydroxyphenyl)-4-nitropyrazol-5(3H)-one by spectroscopic and quantum-chemical methods

The structure of the previously synthesized 1,2-dihydro-3-(2-hydroxyphenyl)-4-nitropyrazol-5(3H)-one (I) was studied by ¹H and ¹³C NMR, IR, and electronic spectra. It was established that the NMR spectra of compound (I) do not contain signals for the H atom at position 4 and the C atoms of the carbonyl groups; in the crystalline state and in solutions the IR spectra do not contain v_c=o bands, while the electronic spectra do not contain absorption in the region of 250 nm. On the basis of the foregoing it is concluded that compound (I) exists in the OH form. The distribution of -electron density in the molecule of (I) and the nature of the bands in its electronic absorption spectrum were studied by quantum-chemical methods in the PPP approximation.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1510–1516, November, 1990.