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2007 1
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2019 2
2020 0
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15 results
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Page 1
Microporous Materials Based on Norbornadiene-Based Cross-Linked Polymers.
Alentiev DA, Dzhaparidze DM, Gavrilova NN, Shantarovich VP, Kiseleva EV, Topchiy MA, Asachenko AF, Gribanov PS, Nechaev MS, Legkov SA, Bondarenko GN, Bermeshev MV. Alentiev DA, et al. Among authors: nechaev ms. Polymers (Basel). 2018 Dec 13;10(12):1382. doi: 10.3390/polym10121382. Polymers (Basel). 2018. PMID: 30961307 Free PMC article.
Making endo-cyclizations favorable again: a conceptually new synthetic approach to benzotriazoles via azide group directed lithiation/cyclization of 2-azidoaryl bromides.
Ageshina AA, Chesnokov GA, Topchiy MA, Alabugin IV, Nechaev MS, Asachenko AF. Ageshina AA, et al. Among authors: nechaev ms. Org Biomol Chem. 2019 May 8;17(18):4523-4534. doi: 10.1039/c9ob00615j. Org Biomol Chem. 2019. PMID: 30994147
Evidence for Indirect Action of Ionizing Radiation in 18-Crown-6 Complexes with Halogenous Salts of Strontium: Simulation of Radiation-Induced Transformations in Ionic Liquid/Crown Ether Compositions.
Zakurdaeva OA, Nesterov SV, Sokolova NA, Dorovatovskii PV, Zubavichus YV, Khrustalev VN, Asachenko AF, Chesnokov GA, Nechaev MS, Feldman VI. Zakurdaeva OA, et al. Among authors: nechaev ms. J Phys Chem B. 2018 Feb 15;122(6):1992-2000. doi: 10.1021/acs.jpcb.7b11498. Epub 2018 Feb 5. J Phys Chem B. 2018. PMID: 29328650
Mixed er-NHC/phosphine Pd(ii) complexes and their catalytic activity in the Buchwald-Hartwig reaction under solvent-free conditions.
Ageshina AA , Sterligov GK , Rzhevskiy SA , Topchiy MA , Chesnokov GA , Gribanov PS , Melnikova EK , Nechaev MS , Asachenko AF , Bermeshev MV . Ageshina AA , et al. Among authors: nechaev ms. Dalton Trans. 2019 Mar 14;48(10):3447-3452. doi: 10.1039/c9dt00216b. Epub 2019 Feb 22. Dalton Trans. 2019. PMID: 30793148
A general method of Suzuki-Miyaura cross-coupling of 4- and 5-halo-1,2,3-triazoles in water.
Gribanov PS, Chesnokov GA, Topchiy MA, Asachenko AF, Nechaev MS. Gribanov PS, et al. Among authors: nechaev ms. Org Biomol Chem. 2017 Nov 22;15(45):9575-9578. doi: 10.1039/c7ob02091k. Org Biomol Chem. 2017. PMID: 29114680
Eight-membered-ring diaminocarbenes bearing naphthalene moiety in the backbone: DFT studies, synthesis of amidinium salts, generation of free carbene, metal complexes, and solvent-free copper catalyzed azide-alkyne cycloaddition (CuAAC) reaction.
Chesnokov GA, Topchiy MA, Dzhevakov PB, Gribanov PS, Tukov AA, Khrustalev VN, Asachenko AF, Nechaev MS. Chesnokov GA, et al. Among authors: nechaev ms. Dalton Trans. 2017 Mar 27;46(13):4331-4345. doi: 10.1039/c6dt04484k. Dalton Trans. 2017. PMID: 28281713
Pursuing reliable thermal analysis techniques for energetic materials: decomposition kinetics and thermal stability of dihydroxylammonium 5,5'-bistetrazole-1,1'-diolate (TKX-50).
Muravyev NV, Monogarov KA, Asachenko AF, Nechaev MS, Ananyev IV, Fomenkov IV, Kiselev VG, Pivkina AN. Muravyev NV, et al. Among authors: nechaev ms. Phys Chem Chem Phys. 2016 Dec 21;19(1):436-449. doi: 10.1039/c6cp06498a. Phys Chem Chem Phys. 2016. PMID: 27905609
Expanded-ring N-heterocyclic carbenes efficiently stabilize gold(I) cations, leading to high activity in π-acid-catalyzed cyclizations.
Morozov OS, Lunchev AV, Bush AA, Tukov AA, Asachenko AF, Khrustalev VN, Zalesskiy SS, Ananikov VP, Nechaev MS. Morozov OS, et al. Among authors: nechaev ms. Chemistry. 2014 May 12;20(20):6162-70. doi: 10.1002/chem.201303760. Epub 2014 Mar 28. Chemistry. 2014. PMID: 24682976
Mechanisms in the reaction of palladium(II)-pi-allyl complexes with aryl halides: evidence for NHC exchange between two palladium complexes.
Normand AT, Nechaev MS, Cavell KJ. Normand AT, et al. Among authors: nechaev ms. Chemistry. 2009 Jul 20;15(29):7063-73. doi: 10.1002/chem.200900373. Chemistry. 2009. PMID: 19575424
Dual reactivity of N-heterocyclic carbenes towards copper(II) salts.
Kolychev EL, Shuntikov VV, Khrustalev VN, Bush AA, Nechaev MS. Kolychev EL, et al. Among authors: nechaev ms. Dalton Trans. 2011 Mar 28;40(12):3074-6. doi: 10.1039/c0dt01630f. Epub 2011 Feb 17. Dalton Trans. 2011. PMID: 21327287
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