Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Ivan V. Glukhov"'
Autor:
Dmitrii M. Roitershtein, Pavel A. Belyakov, Ivan V. Glukhov, A. A. Mikhaylyuk, Konstantin A. Lyssenko, Mikhail E. Minyaev
Publikováno v:
Russian Chemical Bulletin. 61:1726-1732
Reaction of LnCl3(thf)x (Ln = Y, La, Yb, Lu) with NaCpPhn (CpPhn = 1,3-Ph2C5H3, 1,2,4-Ph3C5H2, Ph4C5H) leads to formation of monocyclopentadienyl dichloride complexes Yb(Ph2C5H3)Cl2(thf)3 (1), Ln(Ph3C5H2)Cl2(thf)3 (Ln = Y (2), Lu (3)), La(Ph4C5H)Cl2(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cba2aa6c9b7637412979b56a8802330f
https://doi.org/10.1007/s11172-012-0238-8
https://doi.org/10.1007/s11172-012-0238-8
Autor:
Maxim A. Bastrakov, A. M. Starosotnikov, Ivan V. Glukhov, Svyatoslav A. Shevelev, S. Yu. Pechenkin
Publikováno v:
Russian Chemical Bulletin. 61:74-77
A number of new tetrahydroisoindole derivatives fused with the furazan ring were synthesized based on the 1,3-dipolar cycloaddition of N-methylazomethine ylide with substituted 4-nitrobenzofurazans. Substituents in the benzene ring were found to affe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::643aa03040569677e2e99dd615b37a62
https://doi.org/10.1007/s11172-012-0011-z
https://doi.org/10.1007/s11172-012-0011-z
Autor:
Vasily V. Krivykh, Ivan V. Glukhov, Kamil I. Utegenov, Pavel V. Petrovskii, Nikolay A. Ustynyuk
Publikováno v:
Journal of Organometallic Chemistry. 696:3408-3414
The addition of phosphines to the manganese allenylidene complexes Cp(CO) 2 Mn C C C(Ph)R (R = H, Ph) proceeds selectively at the C α atom to result in the α-phosphonioallenyl complexes Cp(CO) 2 Mn − –C( + PR 3 1 ) C C(Ph)R. The protonation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22cd6a2641a0a9c00808596dfe774680
https://doi.org/10.1016/j.jorganchem.2011.07.034
https://doi.org/10.1016/j.jorganchem.2011.07.034
Autor:
E. S. Taits, Dmitry A. Valyaev, Ivan V. Glukhov, Nikolai A. Ustynyuk, Andrei M. Mazhuga, Vasily V. Krivykh, Pavel V. Petrovskii, Oleg V. Semeikin, Ivan A. Godovikov, Kamil I. Utegenov
Publikováno v:
European Journal of Inorganic Chemistry. 2011:201-211
Stereoselective addition of tertiary phosphanes to manganese and rhenium phenylvinylidenes (η5-C5H5)(CO)2M=C=C(H)Ph (1 M = Mn; 2 M = Re) gave the corresponding zwitterionic Z-phosphoniostyryl adducts (η5-C5H5)(CO)2M−−C(+PR3)=C(H)Ph (3 M = Mn, P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::262f9096a21f04346a917075674173e6
https://doi.org/10.1002/ejic.201000868
https://doi.org/10.1002/ejic.201000868
Autor:
Maxim A. Bastrakov, Svyatoslav A. Shevelev, Alexey M. Starosotnikov, Ivan V. Glukhov, Vadim V. Kachala, Sergey Yu. Pechenkin
Publikováno v:
Journal of Heterocyclic Chemistry. 47:893-896
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a530b41104165496640f384202a5c824
https://doi.org/10.1002/jhet.423
https://doi.org/10.1002/jhet.423
Autor:
Dmitry S. Perekalin, Evgeniya A. Trifonova, Ivan V. Glukhov, Alexander R. Kudinov, Josef Holub
Publikováno v:
Collection of Czechoslovak Chemical Communications. 75:1139-1148
Reaction of the tricarbollide anion [7,8,9-C3B8H11]– (1a) with the naphthalene complex [CpRu(C10H8)]+ under visible light irradiation in CH2Cl2 gives the 12-vertex closo-ruthenacarborane 1-Cp-1,2,3,5-RuC3B8H11 (2; 87% yield). This complex was also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffc0b72df05228c3dcc1ada9e27bbe3f
https://doi.org/10.1135/cccc2010057
https://doi.org/10.1135/cccc2010057
Autor:
Yu. V. Nelyubina, K. A. Lyssenko, Ivan V. Glukhov, Angelina N. Kravchenko, Galina A. Gazieva, Nina N. Makhova, A. S. Sigachev, Marina I. Struchkova
Publikováno v:
Russian Chemical Bulletin. 58:1945-1954
α-Thioureidoalkylation of urea heteroanalogs such as thiosemicarbazide, amino-guanidine, sulfamide, and sulfonamides with 4,5-dihydroxyimidazolidine-2-thiones has been studied. Previously unknown 4,5-bis[thiosemicarbazido(guanidinoamino)]imidazolidi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f576fbf9c165680ab8a81dc90ed92eb9
https://doi.org/10.1007/s11172-009-0266-1
https://doi.org/10.1007/s11172-009-0266-1
Autor:
Leonard M. Khalilov, M. Yu. Antipin, D. V. Nedopekin, G. F. Krainova, Ivan V. Glukhov, R. G. Savchenko, Aleksander G. Tolstikov, Odinokov Viktor N, Vladimir A. Glushkov
Publikováno v:
Russian Chemical Bulletin. 58:1991-1995
Ozonation of N-acyl-4-phenyl-3a,4,5,9b-tetrahydro-3 H-cyclopenta[ c]quinoline gave stable ozonides: a conformationally mobile isomer with the pseudoequatorial N-acyl group and a conformationally stable isomer with the pseudoaxial N-trifluoroacetyl gr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84e2886cef611c1e326665c6c0393198
https://doi.org/10.1007/s11172-009-0272-3
https://doi.org/10.1007/s11172-009-0272-3
Autor:
Zoya A. Starikova, Vladimir I. Bregadze, Irina P. Beletskaya, Ivan V. Glukhov, Sergey N. Mukhin, Kuanysh Kabytaev
Publikováno v:
Organometallics. 28:4758-4763
For the first time, the palladium-catalyzed etheration of 2-iodo-p-carborane with phenolates and alkoxides has been demonstrated. The reactions of 2-iodo-1,12-dicarba-closo-dodecaborane (2-iodo-p-c...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::257232a49a7e4db8027628a7acaadfe4
https://doi.org/10.1021/om9001044
https://doi.org/10.1021/om9001044
Autor:
Maxim A. Bastrakov, A. M. Starosotnikov, Ivan V. Glukhov, Vadim V. Kachala, Svyatoslav A. Shevelev
Publikováno v:
Russian Chemical Bulletin. 58:414-420
Tricyclic heteroaromatic systems of the furoxan, vic-triazole, imidazole, and pyrazine series containing the annulated indazole fragment were synthesized based on substituted aminoindazoles prepared by the functionalization of 4-R-6-nitro-1-phenylind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6866d10ac2785a11251265ca0470b484
https://doi.org/10.1007/s11172-010-0025-3
https://doi.org/10.1007/s11172-010-0025-3