Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Orudzh G. Nabiev"'
Autor:
Remir G. Kostyanovsky, Yuri A. Strelenko, Vasily R. Kostyanovsky, Orudzh G. Nabiev, Konstantin A. Lyssenko, Ivan V. Fedyanin, Gulnara K. Kadorkina, Oleg R. Malyshev
Publikováno v:
Mendeleev Communications. 14:315-318
The enantiomers of asymmetric nitrogen compound 1 have been resolved; a chiral formal meso-form of diaziridine 2 has been obtained; a population of 1,2-cis-form 6a in solution has been found; and the crystal structures of 3–6 have been studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ff5408f6848e756ea13bb33589253ac
https://doi.org/10.1070/mc2004v014n06abeh002083
https://doi.org/10.1070/mc2004v014n06abeh002083
Publikováno v:
Mendeleev Communications. 19:281-283
Simple and efficient methods have been developed to obtain cyanomethylamines and azidomethylamines using reactions of methoxymethylamines with TMSCN and TMSN 3 , respectively. In the case of dimethylformamide dimethylacetal, only one MeO group was su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a28058a29daf8116f02424d398ede46
https://doi.org/10.1016/j.mencom.2009.09.018
https://doi.org/10.1016/j.mencom.2009.09.018
Autor:
Olga V. Dorofeeva, Orudzh G. Nabiev, Ekaterina P. Altova, Alexander V. Mitin, Heinz Oberhammer, Nikolai M. Karasev, Lev V. Vilkov
Publikováno v:
Physical chemistry chemical physics : PCCP. 13(4)
Gas-phase electron-diffraction data and high-level quantum chemical calculations have been used to study the conformational behaviour of N-azidomethylpyrrolidine. The two most stable conformers with a relative abundance of about 80% at 298 K possess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e6bbd23093b4a27a70317cb75170005
https://pubmed.ncbi.nlm.nih.gov/21140015
https://pubmed.ncbi.nlm.nih.gov/21140015
Publikováno v:
ChemInform. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddf28656bc33f36a95476734b2c1f2f4
https://doi.org/10.1002/chin.201006059
https://doi.org/10.1002/chin.201006059
Autor:
Remir G. Kostyanovsky, N.M. Karasev, Orudzh G. Nabiev, Ekaterina P. Altova, Leonid S. Khaikin, Igor F. Shishkov
Publikováno v:
Mendeleev Communications. 23:166-167
As found experimentally (gas-phase electron diffraction) and theoretically, the equilibrium conformers of N -azidomethyl- N , N -dimethylamine are stabilized by anomeric effects.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba0f483ec028d542bb59092c0dbc6a57
https://doi.org/10.1016/j.mencom.2013.05.016
https://doi.org/10.1016/j.mencom.2013.05.016
Publikováno v:
Mendeleev Communications. 20:291-292
Chiroptical properties and X-ray diffraction were studied for both diastereomers of N-[(R)-1-phenylethyl]-2-(3,5-di-tert-butyl-4-hydroxyphenyl)propanamide, whose acid moiety is a chiral antioxidant.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb0a8ca4292309975085699dc8680462
https://doi.org/10.1016/j.mencom.2010.09.018
https://doi.org/10.1016/j.mencom.2010.09.018
Autor:
Gulnara K. Kadorkina, Remir G. Kostyanovsky, Yulia V. Nelyubina, Alexander F. Pozharskii, Orudzh G. Nabiev, Ivan I. Chervin, Konstantin A. Lyssenko, Alexander V. Degtyarev
Publikováno v:
Mendeleev Communications. 18:86-87
By the spontaneous resolution of racemic compound 1,8-bis(dimethylamino)-2-(α-hydroxy-α-phenylethyl)naphthalene (±)-1, enantiomer (–)-1 was obtained; its treatment with C5H5N·HBr resulted in the formation of proton sponge (–)-2; the absolute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::402f15e0d3d75111a0673b37eb56d2ab
https://doi.org/10.1016/j.mencom.2008.03.011
https://doi.org/10.1016/j.mencom.2008.03.011
Autor:
Ivan S. Bushmarinov, Konstantin A. Lyssenko, Mikhail Yu. Antipin, Remir G. Kostyanovsky, Orudzh G. Nabiev
Publikováno v:
CrystEngComm. 13:2930
The geometrical preferences of hydrogen bonds with azide anion are studied using topological analysis of experimental and calculated electron density distribution. The comparison of electron localization function (ELF) and QTAIM analysis shows the re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd90d35bdb545789bdb14d08d39993ba
https://doi.org/10.1039/c0ce00859a
https://doi.org/10.1039/c0ce00859a