Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Dmitriy M. Panov"'
Autor:
Kateryna Znovjyak, Sergiu Shova, Dmitriy M. Panov, Nataliia S. Kariaka, Igor O. Fritsky, Sergey O. Malinkin, Maksym Seredyuk
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 80, Iss 11, Pp 1235-1239 (2024)
The unit cell of the title compound, [Ni(C16H10ClN6)2]·2CH3OH, consists of a neutral complex and two methanol molecules. In the complex, the two tridentate 2-(3-(4-chlorophenyl)-1H-1,2,4-triazol-5-yl)-6-(1H-pyrazol-1-yl)pyridine ligands coordinate t
Externí odkaz:
https://doaj.org/article/c5470dcf90ac4997934c7908f883d40b
Autor:
Yurii S. Moroz, Andrey A. Tolmachev, Sergey E. Pipko, Anzhelika I. Konovets, Pavel K. Mykhailiuk, Dmitriy M. Panov, Andrey V. Bogolubsky
Publikováno v:
ACS Combinatorial Science. 16:375-380
A parallel reductive amination of heteroaromatic amines has been performed using a combination of ZnCl2-TMSOAc (activating agents) and NaBH(OAc)3 (reducing agent). A library of diverse secondary amines was easily prepared on a 50-300 mg scale.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50a0765864f426b0b71849fbe2908a15
https://doi.org/10.1021/co5000568
https://doi.org/10.1021/co5000568
Autor:
Andrey S. Plaskon, Sergey V. Ryabukhin, Oleg Lukin, Alexander Shivanyuk, Dmitriy M. Panov, Evgeniy N. Zarudnitskiy
Publikováno v:
Synthesis. 46:2079-2084
A total of 20 α-aminophosphonic acids are synthesized in 73–89% yields via a one-pot, three-step procedure involving chlorotrimethylsilane-promoted condensation of carbonyl compounds and primary amines yielding azomethine intermediates, subsequent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1328f70573385ed1662d17373363cb22
https://doi.org/10.1055/s-0033-1341064
https://doi.org/10.1055/s-0033-1341064
Autor:
Roman Doroschuk, Anzhelika I. Konovets, Sergey E. Pipko, Yurii S. Moroz, Andrey V. Bogolubsky, Andrey A. Tolmachev, Dmitriy M. Panov
Publikováno v:
Synthesis. 46:1765-1772
A combination of a condensation mixture [a Lewis acid, Ti(Oi-Pr)4, and a water scavenger, 1-(trimethylsilyl)-2-pyrrolidinone] and a simple reductant (NaBH4) provides an efficient one-pot approach to parallel synthesis of secondary amines by the reduc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb4936851030615ac70bbf7449cf2dff
https://doi.org/10.1055/s-0033-1341226
https://doi.org/10.1055/s-0033-1341226
Autor:
Andrey A. Tolmachev, Sergey V. Ryabukhin, Alexander Shivanyuk, Dmitriy M. Panov, Sergey E. Pipko, Andrey S. Plaskon, Alexander Chuprina
Publikováno v:
Molecular Diversity. 16:625-637
128 Azomethines were synthesized through condensation of carbonyl compounds with various amines in pyridine in the presence of Me(3)SiCl as promoter and water scavenger in 58-98 % yield. Et(3)N was added to reaction mixtures before precipitating the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d6a929d953eb9f984241fc252f98d46
https://doi.org/10.1007/s11030-012-9407-9
https://doi.org/10.1007/s11030-012-9407-9
Autor:
Radomyr V. Smaliy, Andrey A. Tolmachev, Dmitriy M. Panov, Andrey S. Plaskon, Sergey V. Ryabukhin
Publikováno v:
Monatshefte für Chemie - Chemical Monthly. 143:1507-1517
Chlorotrimethylsilane has been found to be an efficient condensing agent in the Pictet–Spengler reaction, affording an extremely straightforward synthetic route to tetrahydro-β-carboline derivatives and their analogs. The applicability of the meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e5615dd807abc8d17f7c8c257b2d9b7
https://doi.org/10.1007/s00706-012-0804-7
https://doi.org/10.1007/s00706-012-0804-7
Autor:
Aleksandr A. Yurchenko, Dmitriy M. Panov, Dmitriy M. Volochnyuk, Igor I. Pervak, Alexander Shivanyuk, Pavel V. Khodakovskiy, Andrey A. Tolmachev, Oleg V. Shishkin, Evgenij V. Zarudnitskii
Publikováno v:
Synthesis. 2008:948-956
A facile method of trifluoroacylation of imidazoles, 1,3-thiazoles, and 1,3-oxazoles with trifluoroacetic anhydride resulted in a set of heterocyclic trifluoromethyl-containing ketones. Unlike common ketones, these compounds form stable hydrates and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e68c4caccbbbf83cfc3d1b433e5111d
https://doi.org/10.1055/s-2008-1032197
https://doi.org/10.1055/s-2008-1032197
Autor:
Dmitriy M. Panov, Andrey V. Bogolubsky, Anzhelika I. Konovets, Roman Doroschuk, Sergey E. Pipko, Yurii S. Moroz, Andrey A. Tolmachev
Publikováno v:
ChemInform. 45
A set of arbitrarily chosen acyclic and cyclic, alkyl and aryl ketones as well as amines (twenty each) are converted in this one-pot approach to build up a library of secondary amines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10eda5c611e7aa827d96e5896ee0f31b
https://doi.org/10.1002/chin.201452065
https://doi.org/10.1002/chin.201452065
Autor:
Oleksandr O. Grygorenko, Eugeniy N. Ostapchuk, Dmitry S. Granat, Dmitriy M. Panov, Sergey V. Ryabukhin, Dmitriy V. Kryvoruchko
Publikováno v:
ACS combinatorial science. 16(3)
One-pot variation of Castagnoli condensation, that is, reaction of cyclic anhydrides, amines, and aldehydes, has been developed as a combinatorial approach to 1,2-disubstituted 5-oxopyrrolidine- and 6-oxopiperidine-3-carboxylic acids, as well as thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcac949e324ffcc9bd73c3f2f2b698c8
https://pubmed.ncbi.nlm.nih.gov/24479637
https://pubmed.ncbi.nlm.nih.gov/24479637
Autor:
Radomyr V. Smaliy, Andrey A. Tolmachev, Sergey V. Ryabukhin, Andrey S. Plaskon, Dmitriy M. Panov
Publikováno v:
ChemInform. 44
A variety of tetrahydro-β-carbolines and their analogues is readily prepared by chlorotrimethylsilane-promoted Pictet—Spengler reaction (33 examples).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40e5dfa6e92da0ad77debabfd47e3713
https://doi.org/10.1002/chin.201307142
https://doi.org/10.1002/chin.201307142