Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Ivan S, Golovanov"'
Autor:
Vladislav K. Lesnikov, Ivan S. Golovanov, Yulia V. Nelyubina, Svetlana A. Aksenova, Alexey Yu. Sukhorukov
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Despite the rich coordination chemistry, hydroxylamines are rarely used as ligands for transition metal coordination compounds. This is partially because of the instability of these complexes that undergo decomposition, disproportionation an
Externí odkaz:
https://doaj.org/article/6529ebd503c94fc2bc4cc0f84bc5d7e1
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 1424-1434 (2022)
A synthetic route to 1,4,6,10-tetraazaadamantanes (TAADs) bearing free and protected amino groups at the bridge N-atoms has been developed via intramolecular cyclotrimerization of C=N units in the corresponding tris(hydrazonoalkyl)amines. In a simila
Externí odkaz:
https://doaj.org/article/a7d1a625d90549018946b8ffe90d2e00
Autor:
Nikita S. Gudim, Ekaterina A. Knyazeva, Ludmila V. Mikhalchenko, Ivan S. Golovanov, Vadim V. Popov, Natalia V. Obruchnikova, Oleg A. Rakitin
Publikováno v:
Molecules, Vol 26, Iss 16, p 4931 (2021)
This paper presents an improved synthesis of 4,7-dibromobenzo[d][1,2,3]thiadiazole from commercially available reagents. According to quantum-mechanical calculations, benzo[d][1,2,3]thiadiazole (isoBTD) has higher values of ELUMO and energy band gap
Externí odkaz:
https://doaj.org/article/445e23f0685647989fdd630cb8a147d1
Publikováno v:
Molecules, Vol 25, Iss 16, p 3613 (2020)
An efficient asymmetric synthesis of GlaxoSmithKline’s potent PDE4 inhibitor was accomplished in eight steps from a catechol-derived nitroalkene. The key intermediate (3-acyloxymethyl-substituted 1,2-oxazine) was prepared in a straightforward manne
Externí odkaz:
https://doaj.org/article/006be05a8e17462888e0d1a4ece5f649
Autor:
Ivan S. Golovanov, Yulia V. Nelyubina, Alexey Yu. Sukhorukov, Sema L. Ioffe, Roman S. Malykhin
Publikováno v:
The Journal of Organic Chemistry. 86:16337-16348
Reaction of six-membered cyclic nitronates with disubstituted ketenes affords hitherto unknown saturated oxazolo[3,2-b][1,2]oxazines possessing up to four contiguous stereogenic centers. The process involves a tandem of [3+2]-cycloaddition across the
Autor:
Ivan S. Golovanov, Anton V. Leonov, Vladislav K. Lesnikov, Evgeny V. Pospelov, Kirill V. Frolov, Alexander A. Korlyukov, Yulia V. Nelyubina, Valentin V. Novikov, Alexey Yu. Sukhorukov
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 51(11)
4,6,10-Trihydroxy-1,4,6,10-tetraazaadamantane (TAAD) has been shown to form a stable Fe(IV) complex having a diamantane cage structure, in which the metal center is coordinated by three oxygen atoms of the deprotonated ligand. The complex was charact
Autor:
Roman S, Malykhin, Ivan S, Golovanov, Yulia V, Nelyubina, Sema L, Ioffe, Alexey Yu, Sukhorukov
Publikováno v:
The Journal of organic chemistry. 86(23)
Reaction of six-membered cyclic nitronates with disubstituted ketenes affords hitherto unknown saturated oxazolo[3,2
Autor:
Vladislav M. Korshunov, Timofey N. Chmovzh, Alexandra Ya Freidzon, Mikhail E. Minyaev, Artem D. Barkanov, Ivan S. Golovanov, Lyudmila V. Mikhalchenko, Igor C. Avetisov, Ilya V. Taydakov, Oleg A. Rakitin
Publikováno v:
Dyes and Pigments. 208:110860
Autor:
Nikita S, Gudim, Ekaterina A, Knyazeva, Ludmila V, Mikhalchenko, Ivan S, Golovanov, Vadim V, Popov, Natalia V, Obruchnikova, Oleg A, Rakitin
Publikováno v:
Molecules
This paper presents an improved synthesis of 4,7-dibromobenzo[d][1,2,3]thiadiazole from commercially available reagents. According to quantum-mechanical calculations, benzo[d][1,2,3]thiadiazole (isoBTD) has higher values of ELUMO and energy band gap
Publikováno v:
IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA. 62:60-67
In this article synthesis of stable ate complexes of heteroaromatic boronic acids and 4,6,10-trihydroxy-1,4,6,10-tetraazaadamantane is described. Ate complexes that have betaine structure were prepared by reaction of tris(β-oximinomethyl)amine with