MAJOR PUBLICATIONS BY N. S. ZEFIROV FOR THE LAST 10 YEARS
N. V. Averina, G. S. Borisova, O. N. Zefirova, E. V. Selyunina, N. V. Zyk, and N. S. Zefirov, “Synthetic approaches to physiologically active polycyclic compounds: III. Ritter reaction with ketones of the adamantane and oxahomoadamantane series,” Zh. Org. Khim., 40, 528–532 (2004).
A. S. Dudnik, A. V. Ivanov, L. G. Tomilova, and N. S. Zefirov, “Synthesis and study of ruthenium phthalocyanine complexes,” Koordinats. Khim., 30(2), 120–124 (2004).
R. G. Gafurov and N. S. Zefirov, “Strategy of chemical designing of phytoregulators and stress protectors with the given properties,” Dokl. Akad. Nauk, 399, 422–424 (2004).
I. G. Tikhonova, I. I. Baskin, V. A. Palyulin, and N. S. Zefirov, “3D-Model of the NMDA receptor ion channel. Qualitative and quantative modeling of binding of channel blockers,” Dokl. Akad. Nauk, 396, 551–556 (2004).
I. G. Tikhonova, I. I. Baskin, V. A. Palyulin, and N. S. Zefirov, “Molecular modeling of N-terminal domains of NMDA-receptor, ligand biding study with N-thermal domains,” Dokl. Akad. Nauk, 397, 549–557 (2004).
M. S. Belenikin, G. Konstantino, V. A. Palyulin, R. Pellichari, and N. S. Zefirov, “Molecular modeling of the transmembrane domain of the metabotropic glutamate receptor mGluR1 and the model of its dimeric form,” Dokl. Akad. Nauk, 393, 827–831 (2003).
O. B. Bondarenko, A. Yu. Gavrilova, L. G. Saginova, N. V. Zyk, and N. S. Zefirov, “Δ 2-Isoxazolines from arylcyclopropanones: reaction with nitrosyl chloride, activated with sulfur trioxide,” Izv. Akad. Nauk. Ser. Khim., 741–742 (2003).
E. M. Budynina, O. A. Ivanova, E. B. Averina, T. S. Kuznetsova, and N. S. Zefirov, “Formation of 2,2-dinitropiperidin-4-ones in the addition of tetranitromethane to bicyclobutylidene and methylenecyclopropanes,” Zh. Org. Khim., 39, 783–785 (2003).
N. M. Gal'bershtam, I. I. Baskin, V. A. Palyulin, and N. S. Zefirov, “Neuron networks as method for the search for structure-property relationships in organic compounds,” Usp. Khim., 72, 706–727 (2003).
G. V. Grishina, A. A. Borisenko, Z. G. Nosan', I. S. Veselov, L. D. Ashkinadze, E. V. Karamov, G. V. Kornilaeva, and N. S. Zefirov, “trans-Dihydroxypiperidines. Synthesis, stereochemistry, and anti-HIV-1 activity,” Dokl. Akad. Nauk, 391, 487–391 (2003).
A. V. Ivanov, P. A. Svinareva, I. V. Zhukov, L. G. Tomilova, and N. S. Zefirov, “New phthalocyanine complexes based on 4,5-isopropylidenedioxyphthalonitrile,” Izv. Akad. Nauk. Ser. Khim., 1479–1483 (2003).
N. A. Lozinskaya, V. V. Tsybezova, M. V. Proskurnina, and N. S. Zefirov, “Synthesis of cis-and trans-2,4,5-triarylimidazolines and 2,4,5-triarylimidazoles from simple reagents,” Izv. Akad. Nauk. Ser. Khim., 646–650 (2003).
S. S. Mochalov, R. A. Gazzaeva, A. N. Fedotov, Yu. S. Shabarov, and N. S. Zefirov, A new route to substituted 4H-3,1-benzoxazines, Khim. Geterotsikl. Soedin., 922–929 (2003).
A. Yu. Maksimov, A. V. Ivanov, Yu. N. Blikova, L. G. Tomilova, and N. S. Zefirov, “Synthesis and spectroscopic characterization of planar binuclear nickel(II) hexa(tert-butyl)phthalocyaninate,” Mendeleev Commun., 70–72 (2003).
E. V. Trofimova, A. N. Fedotov, R. A. Gazzaeva, S. S. Mochalov, Yu. S. Shabarov, and N. S. Zefirov, “Heterocyclic ions from the N-oxides of N-(4-nitrobenzylidene)-2-cyclopropyl-and N-(4-nitrobenzylidene)-2-cyclopropylmethylanilines: formation, isomerization, and transformations,” Khim. Geterotsikl. Soedin., 234–242 (2003).
I. I. Brunovlenskova, E. D. Matveeva, T. A. Podrugina, V. A. Palyulin, and N. S. Zefirov, “A new approach to the synthesis of bioisosteric analogues of nicotine,” Vestn. MGU, Ser. Khim., 43, 248–250 (2002).
N. V. Averina, T. V. Lapina, O. N. Zefirova, and N. S. Zefirov, “Synthesis of compounds with potential anticancer activity. II. Synthesis of 1-amino-4-oxahomoadamantanane-5-on by Ritter reaction,” Vestn. MGU, Ser. Khimiya, 43, 244–246 (2002).
O. A. Ivanova, E. B. Averina, Yu. K. Grishin, T. S. Kuznetsova, A. A. Korlyukov, M. Yu. Antipin, and N. S. Zefirov, “Study of 4-hydroxy-3-nitroisoxazoline N-oxide in 1,3-dipolar cycloaddition to olefins containing small rings,” Dokl. Akad. Nauk, 382, 349–352 (2002).
N. Sh. Pirkuliev, V. K. Brel', V. V. Zhdankin, and N. S. Zefirov, “Reaction of fluoro[trifluoromethanesulfonyloxy-3-iodanil]benzene with nitrogen-containing heterocycles,” Zh. Org. Khim., 38, 1275–1276 (2002).
E. G. Kogan, A. V. Ivanov, L. G. Tomilova, and N. S. Zefirov, “Synthesis of mono-and bisphthalocyanine complexes using microwave irradiation,” Mendeleev Commun., 54–55 (2002).
M. I. Skvortsova, K. S. Fedyaev, I. I. Baskin, V. A. Palyulin, and N. S. Zefirov, “New method for chemical structure coding with the use of basic fragments,” Dokl. Akad. Nauk, 382, 645–648 (2002).
E. M. Budynina, N. V. Yashin, O. A. Ivanova, E. B. Averina, T. S. Kuznetsova, R. V. Shpachenko, and N. S. Zefirov, “The reaction of cyclopropane-1,1-dycarboxylic acid diethyl ether with hydrazine hydrate. The synthesis and the crystal structure of 1-N-amino-2-oxopyrrolidine-3-carboxylic acid hydrazide,” Dokl. Akad. Nauk, 381, 63–65 (2001).
N. V. Averina, G. S. Borisova, and N. S. Zefirov, “Advances in the chemistry of 4-Azatricyclo[4.3.1.13,8]undecane (4-azahomoadamantane) derivatives,” Zh. Org. Khim., 37, 959–986 (2001).
A. V. Leont'ev, O. A. Fomicheva, M. V. Proskurnina, and N. S. Zefirov, “Modern chemistry of nitrogen(I) oxide,” Usp. Khim., 107–121 (2001).
O. N. Zefirova and N. S. Zefirov, “Physiologically active compounds interacting with glutamate receptors,” Zh. Org. Khim., 36, 1273–1300 (2000).
O. A. Ivanova, E. B. Averina, T. S. Kuznetsova, and N. S. Zefirov, “Synthesis of new 3,4-substituted furazans,” Khim. Geterotsikl. Soedin., 1251–1258 (2000).
E. D. Matveeva, T. A. Podrugina, I. G. Morozkin, S. E. Tkachenko, and N. S. Zefirov, “Synthesis and neuroprotector characteristics of isosteric analogs of nicotine,” Khim. Geterotsikl. Soedin., 1330–1334 (2000).
E. V. Trofimova, A. N. Fedotov. S. S. Mochalov, Yu. S. Shabarov, and N. S. Zefirov, “Acid-catalyzed transformations of N-(nitrobenzylidene)-2-cyclopropyl-and N-(4-nitrobenzylidene)-2-alkenylanilines. A new way to the synthesis of dihydroquinolines and quinolines,” Khim. Geterotsikl. Soedin., 1385–1394 (2000).
G. Kornilayeva, G. Grishina, T. Zilbershtein, T. Chumakov, N. Yaroslavtseva, N. Zefirov, and E. Karamov, “Piperidine derivatives suppress virus production under chronic HIV infection,” Russian Journal of HIV/AIDS and Related Problems, 3, No.1, 56 (1999).
S. S. Mochalov, R. A. Gazzaeva V. N. Atanov, A. N. Fedotov, and N. S. Zefirov, “Substituted 2-cyclopropyl-1,4-benzodioxanes in reaction with dinitrogen tetroxide,” Khim. Geterotsikl. Soedin., 324–329 (1999).
L. N. Sobenina, L. A. Es'kova, A. I. Mikhaleva, D. S. Toryashnikova, A. I. Albanov, B. A. Trofimov, and N. S. Zefirov, “Nucleophilic addition of pyrroles to vinyl sulfones,” Zh. Org. Khim., 35, 1226–1231 (1999).
G. V. Grishina, T. I. Chumakov, E. L. Gaidarova, N. S. Zefirov, T. A. Pashkova, and E. V. Karamov, “Anti-HIV activity of functionally substituted piperidine derivatives. The relation of conformation compounds and anti-HIV activity,” Russian Journal of HIV/AIDS and related Problems, 2, No.3, 89 (1998).
F. I. Guseinov, N. A. Yudina, R. N. Burangulova, G. Yu. Klimentova, B. M. Ismailov, A. T. Gubaidullin, I. A. Litvinov, and N. S. Zefirov, “Synthesis and molecular structure of 1,3-diphenyl(dimethyl)-9,9,10,10-tetrachloro-2,4,6,8-tetraoxaadamantanes,” Dokl. Akad. Nauk, 359, 778–781 (1998).
S. S. Mochalov, V. N. Atanov, and N. S. Zefirov, “Behavior of 6-cyclopropyl-and 6-bromo-7-cyclopropyl-1,4-benzodioxanes under conditions of electrophilic reactions,” Khim. Geterotsikl. Soedin., 618–620 (1998).
A. A. Abramov, N. V. Averina, B. Z. Iofa, V. V. Samoshin, N. A. Ivanova, Yu. A. Sapozhnikov, and N. S. Zefirov, “Study of the extraction of strontium(II) and lead(II) by crown and dithiacrown ethers,” Khim. Geterotsikl. Soedin., 1125–1129 (1997).
S. Z. Vatsadze, V. K. Bel'skii, S. E. Sosonyuk, N. V. Zyk, and N. S. Zefirov, “Synthesis and spectra of bispidine complexes with copper(II) chloride and bromide. Molecular and crystal structure of the complexes of 1,5-diphenyl-3,7-di(2-cyanoethyl)bispidone-9 with copper chloride and 1,5-diphenyl-3,7-diallylbispidone-9 with copper bromide,” Khim. Geterotsikl. Soedin., 356–366 (1997).
E. V. Babaev and N. S. Zefirov, “Molecular design of heterocycles. 6. Hetarenes with bridging nitrogen atom. 4. Strategy and tactics for computer prediction of new recyclizations in the series of azolopyridines with a bridging nitrogen atom,” Khim. Geterotsikl. Soedin., 1564–1580 (1996).
I. V. Alabugin, G. A. Sereda, E. V. Abramkin. V. K. Brel', N. V. Zyk, and N. S. Zefirov, “Synthesis of heterocyclic and acyclic derivatives of 1,2-alkadienephosphonic acids with the use of potassium dichloroiodate(I),” Zh. Org. Khim., 32, 1400–1403 (1996).
S. Z. Vatsadze, S. E. Sosonyuk, N. V. Zyk, K. A. Potekhin, O. I. Levina, Yu. T. Struchkov, and N. S. Zefirov, “Molecular and crystal structure of the complex of 3,7-di(2-propenyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonan-9-one with copper(II) chloride,” Khim. Geterotsikl. Soedin., 770–774 (1996).
N. S. Zefirov, V. A. Palyulin, K. A. Potekhin, S. V. Starovoitova, and Yu. T. Struchkov, “Synthesis of 1,11,13,23-tetraphenyl-3,9,15,21-tetraazapentacyclo[19.3.1.13,23.111,15]octacosane-12,24-dione and the crystal and molecular structure of its solvate with acetone,” Dokl. Akad. Nauk, 346, 342–345 (1966).
N. S. Zefirov, V. A. Palyulin, S. V. Starovoitova, K. A. Potekhin, and Yu. T. Struchkov, “Synthesis, crystalline and molecular structure of 3,7-bis(β-hydroxyethyl)-1,5-diphenyl-3,7-diazabicyclo[3.3.1]-nonan-9-one,” Dokl. Akad. Nauk, 347, 637–640 (1996).
S. S. Mochalov, E. V. Trofimova, A. N. Fedotov, Yu. S. Shabarov, and N. S. Zefirov, “Acid-catalyzed transformations of 1-chloro-2-nitrobenzenecyclopropanes. The first stable N-oxo-2,1-benzoxazepinium ions,” Zh. Org. Khim., 32, 852–860 (1996).
V. A. Palyulin, K. A. Potekhin, A. E. Lysov, S. V. Emets, S. V. Starovoitova, N. S. Zefirov, and X.-X. Schneider, “Synthesis and crystal and molecular structure of 3,7-bis[(4-methyl-1-piperazinyl)acetyl]-1,5-diphenyl-3,7-diazabicyclo[3.3.1]nonane,” Dokl. Akad. Nauk, 350, 353–356 (1996).
M. S. Molchanov, V. V. Shcherbukhin, and N. S. Zefirov, “Computer generation of molecular structures by SMOG program,” J. Chem. Information Comput. Sci., 36, 888–899 (1996).
N. S. Zefirov, “Novel reagents of iodine(+III) and sulfur,” Pure Appl. Chem., 68, 881–890 (1996).
S. P. Gromov, O. A. Fedorova, A. I. Vedernikov, V. V. Samoshin, N. S. Zefirov, and M. V. Alfimov, “Synthesis of formyl derivatives of benzocrown ethers containing heteroatoms N, S, O in the macrocycle,” Izv. Akad. Nauk. Ser. Khim., 121–127 (1995).
N. S. Zefirov, V. A. Palyulin, K. A. Potekhin, A. V. Goncharov, S. I. Kozhushkov, and Yu. T. Struchkov, “Crystal and molecular structure of 3,7,9-trioxabicyclo[3.3.1]nonane and 3-oxo-9-oxa-3,7-dithiabicyclo[3.3.1]nonane,” Dokl. Akad. Nauk, 343, 198–201 (1995).
V. L. Lapteva, M. V. Rusalov, V. V. Samoshin, M. A. Kirpichenok, S. I. Druzhinin, V. M. Uzhinov, and N. S. Zefirov, “New fluoroionophores containing coumarin moiety,” Dokl. Akad. Nauk, 344, 200–202 (1995).
V. V. Samoshin, K. V. Kudryavtsev, and N. S. Zefirov, “New thiacrown ethers containing the thioacetal group,” Khim. Geterotsikl. Soedin., 133–134 (1995).
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Nikolai Serafimovich Zefirov Seventieth Birthday. Chem Heterocycl Compd 41, 1085–1090 (2005). https://doi.org/10.1007/s10593-005-0284-3
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DOI: https://doi.org/10.1007/s10593-005-0284-3