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Boris A TrofimovSvetlana F Malysheva Boris G SukhovNatal'ya A Belogorlova Elena Yu SchmidtLyubov N Sobenina Vladimir A KuimovNina K Gusarova 《Tetrahedron letters》2003,44(13):2629-2632
Secondary phosphines 1-3 react readily with N-vinylpyrroles 4 and 5 under radical initiation to give regiospecifically anti-Markovnikov adducts, diorganyl-2-(1-pyrrolyl)ethylphosphines 6a-d, highly reactive building blocks for organic synthesis, in 88-91% yields. 相似文献
3.
S. E. Korostova B. A. Trofimov L. N. Sobenina A. I. Mikhaleva M. V. Sigalov 《Chemistry of Heterocyclic Compounds》1982,18(10):1043-1045
2-(1-Naphthyl)- and 2-(2-naphthyl)pyrroles and their 1-vinyl derivatives were synthesized in 22–64% yields by the reaction of 1- and 2-acetylnaphthalene oximes with acetylene at both atmospheric pressure and elevated pressures in an alkali metal hydroxide-dimethyl sulfoxide system.See [1] for communication 22.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1351–1353, October, 1982. 相似文献
4.
L. N. Sobenina A. I. Mikhaleva M. P. Sergeeva D. -S. D. Toryashchinova O. B. Kozyreva B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1996,32(1):43-47
Condensation of pyrrole-2-dithiocarboxylates with CH acids containing ester groups, in the KOH-DMSO system, was used to prepare previously unknown 1-alkylthio-3H pyrrolizin-3-ones. The latter, treated with secondary amines, are readily converted to the corresponding 1-amino derivatives. 相似文献
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Boris A. Trofimov Ol’ga V. Petrova Lyubov’ N. Sobenina Igor’ A. Ushakov Al’bina I. Mikhaleva Yurii Yu. Rusakov Leonid B. Krivdin 《Tetrahedron letters》2006,47(22):3645-3648
Functionalized pyrrolic enols, 2-(2,2-dicyano-1-hydroxyethenyl)-1-methylpyrroles, synthesized from 2-ethenylpyrroles by a nucleophilic SEt-OH exchange, upon heating (75-142 °C) are readily rearranged to their 3-isomers in near to quantitative yield. The inter or intramolecular auto-protonation of a pyrrole ring by the acidic enol hydroxyl to form a mesomeric pyrrolium cation or zwitterion is suggested to be a key step in the rearrangement. 相似文献
7.
Chipanina N. N. Turchaninov V. K. Vorontsov I. I. Antipin M. Yu. Stepanova Z. V. Sobenina L. N. Mikhaleva A. I. Trofimov B. A. 《Russian Chemical Bulletin》2002,51(1):111-116
The molecular structure of 2-(2-benzoyl-1-phenylethenyl)-5-phenylpyrrole and 2-(2-furoyl-1-phenylethenyl)-5-phenylpyrrole was studied by X-ray diffraction analysis at 110 K and quantum chemistry methods (B3LYP/6-31G*). In the crystalline state, both compounds have cyclic structures closed by strong intramolecular hydrogen bond N—H...O. Canonic zwitterionic structure contributes largely to the ground state of the molecules. This is probably due to synergism of the H-bonding and -electron interactions. 相似文献
8.
L. N. Sobenina A. I. Mikhaleva M. P. Sergeeva D. -S. D. Toryashinova O. B. Kozyrea B. A. Trofimov 《Chemistry of Heterocyclic Compounds》1996,32(7):783-788
Previously unknown 1-alkylthio-3H-pyrrolizin-3-ones have been obtained by the condensation of pyrrole-2-dithiocarboxylates with CH acids containing ester groupings in the KOH-DMSO system. On treating the products with secondary amines they are readily converted into the corresponding 1-amino derivatives.Irkutsk Branch of the Russian Academy of Sciences, Irkutsk 664033. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 919–924, July, 1996. Original article submitted May 2, 1996. 相似文献
9.
Denis N. Tomilin Lyubov N. Sobenina Marina V. Markova Maxim D. Gotsko Igor A. Ushakov Vladimir I. Smirnov 《合成通讯》2013,43(14):1652-1661
5-Acylethynylpyrrole-2-carbaldehydes have been synthesized from the protected pyrrole-2-carbaldehydes by their transition-metal-free topochemical mechanoactivated ethynylation with acylbromoacetylenes in a solid Al2O3 medium (room temperature, 6 h, 41–54% yields). 相似文献
10.
L. N. Sobenina Z. V. Stepanova O. V. Petrova J. Sh. Ma G. Yang A. A. Tatarinova A. I. Mikhaleva B. A. Trofimov 《Russian Chemical Bulletin》2013,62(1):88-92
Cross-coupling of 2-(biphenyl-4-yl)pyrroles derived from 1-(biphenyl-4-yl)ethanone oximes and acetylene with 3-bromo-1-phenylprop-2-yn-1-one on aluminum oxide gave 3-[5-(biphe-nyl-4-yl)pyrrol-2-yl]-1-phenylprop-2-yn-1-ones in 35–46% yields. 相似文献