Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ivan D. Nesterov"'
Publikováno v:
Mendeleev Communications. 31:197-200
Based on a combination of quantum chemistry and atom–atom potentials methods, we developed a technique for modeling the structure and estimating the complexation energy of a binary organic complex in gas and crystal phases. The efficiency of this t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d9f45dbd6de1f5a6749d4adb2138e2c
https://doi.org/10.1016/j.mencom.2021.03.017
https://doi.org/10.1016/j.mencom.2021.03.017
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 50(1)
Thirteen new metallacarborane complexes of rhodium and iridium with covalently bound cage carbon atoms were synthesized and their thermal stability was investigated. Two iridium complexes undergo a polyhedral rearrangement with the formation of more
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9e940c34ba0640efd061a3a08fcd02
https://pubmed.ncbi.nlm.nih.gov/33300519
https://pubmed.ncbi.nlm.nih.gov/33300519
Autor:
Tatyana S. Pivina, Vjacheslav L. Korolev, Ivan D. Nesterov, Vitaliy M. Danilenko, Natalia L. Merkulova
Publikováno v:
Journal of Molecular Structure. 1207:127775
The tautomerism of imidazo[4,5-e]benzo[1,2-c; 3,4-c’]difuroxan in DMSO solution and in a water-acetonitrile system was studied experimentally using 1H, 13C NMR and liquid chromatography - mass spectrometry (LC-MS). The relative thermodynamic stabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f14c5d48e0d0aa8a59a30932e9b148
https://doi.org/10.1016/j.molstruc.2020.127775
https://doi.org/10.1016/j.molstruc.2020.127775
Autor:
Alexander A. Tishkov, Ivan D. Nesterov, Vladimir A. Tartakovsky, Sema L. Ioffe, William A. Smit, Vladimir O. Smirnov, Yulia A. Khomutova, Michael Yu. Antipin
Publikováno v:
ChemInform. 36
Cyclic six-membered nitronates 1 are involved in diastereoselective C-C coupling reactions with various nucleophiles in the presence of either catalytic or stoichiometric amounts of TBDMSOTf to give the previously unknown N-siloxytetrahydrooxazines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dff79c69d95121891f6ec8ac131f2833
https://doi.org/10.1002/chin.200517167
https://doi.org/10.1002/chin.200517167
Publikováno v:
ChemInform. 35
A general and convenient method for the synthesis of the scarcely known 3-α-haloalkyl-5,6-dihydro-4H-1,2-oxazines 2 via siiylation of the corresponding six-membered cyclic nitronates 1 or the first obtained 2-silyloxy-1,2-oxazines 3 by Me 3 SiX/Et 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e56bebb445cda6dfbe17911ac7ed571
https://doi.org/10.1002/chin.200442178
https://doi.org/10.1002/chin.200442178
Autor:
Ivan D. Nesterov, Sema L. Ioffe, Alexey V. Lesiv, Yury A. Strelenko, Michael Yu. Antipin, Yulya A. Khomutova, Scott E. Denmark, Alexander A. Tishkov
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::652a70a6fcd4fac19e866fe1fd79fbcc
https://doi.org/10.1002/chin.200415148
https://doi.org/10.1002/chin.200415148
Autor:
Yulya A. Khomutova, Sema L. Ioffe, Yury A. Strelenko, Michael Yu. Antipin, Scott E. Denmark, A. A. Tishkov, Alexey V. Lesiv, Ivan D. Nesterov
Publikováno v:
The Journal of organic chemistry. 68(24)
3-alkyl-substituted 1,2-oxazine N-oxides 2 can be selectively transformed into 2-silyloxy-1,2-oxazines 1 upon treatment with silylating reagents. In the solid state derivatives 1 adopt a chair conformation with the pyramidal nitrogen atom, whereas in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae1b35da7c760bbb82193fd4ddaadca9
https://pubmed.ncbi.nlm.nih.gov/14629175
https://pubmed.ncbi.nlm.nih.gov/14629175
Publikováno v:
Mendeleev Communications. 14:280-281
The most preferable conformation of 5,6-dihydro-4[H]-oxazines and their N-oxides is a distorted semi-chair, in which only the C(6) atom considerably deviates from the plane of the C=N bond, whereas 'planar' conformations, in which the O-alkyl group i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4ca5ede6f69438f717c774a7bebfb70d
https://doi.org/10.1070/mc2004v014n06abeh002039
https://doi.org/10.1070/mc2004v014n06abeh002039