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 Київський національний університет
імені Тараса Шевченка

Кафедра аналітичної хімії


2014

Наукові статті співробітників кафедри у журналах, що мають імпакт фактор вище за одиницю (IF>1,0)


1.       Mykhalchuk P. K., Babii, O.;Afonin, S.;Berditsch, M.; Reiβer S;Kubyshkin V. S.; Ulrich A. S.; Komarov I. V.
Controlling Biological Activity with Light: Diarylethene-Containing Cyclic Peptidomimetics
Ang.Chem.Int.Ed. 2014, 53, 3392–3395.
IF: 11,34

2.       Mykhalchuk P. K.
In situ-generation of C2F5CHN2 and its first reaction – [3+2]-cycloaddition with alkenes.
Chem. J. 2014, 20, 4942–4947
IF: 5,70

3.       Subramanian, P., Mazurenko, I., Zaitsev, V., Coffinier, Y., Boukherroub, R., & Szunerits, S.
Diamond nanowires modified with poly[3-(pyrrolyl)carboxylic acid] for the immobilization of histidine-tagged peptides.
The Analyst, 2014, 139(17), 4343–9. doi:10.1039/c4an00146j
IF: 3,91

4.       Coffinier, Y., Kurylo, I., Drobecq, H., Szunerits, S., Melnyk, O., Zaitsev, V. N., & Boukherroub, R.
Decoration of silicon nanostructures with copper particles for simultaneous selective capture and mass spectrometry detection of His-tagged model peptide
The Analyst, 2014, 139(20), 5155–63. doi:10.1039/c4an01056f
IF: 3,91

5.       Subramanian, P., Motorina, A., Yeap, W. S., Haenen, K., Coffinier, Y., Zaitsev, V., … Szunerits, S.
An impedimetric immunosensor based on diamond nanowires decorated with nickel nanoparticles.
The Analyst, 2014, 139(7), 1726–31. doi:10.1039/c3an02045b
IF: 3,91

6.       Motorina A., Tananaiko O., Kozytska I., Raks V., Badía R., Díaz-García M.E., Zaitsev V.N.
Hybrid silica–polyelectrolyte films as optical sensing materials for tetracycline antibiotics
Sens. Actuators, B. 2014, 200 (1), 198–205.
IF: 3,84

7.       Turcheniuk, K., Khanal, M., Motorina, A., Subramanian, P., Barras, A., Zaitsev, V., … Szunerits, S.
Insulin loaded iron magnetic nanoparticle–graphene oxide composites: synthesis, characterization and application for in vivo delivery of insulin.
RSC Advances, 2014, 4(2), 865. doi:10.1039/c3ra46307a
IF: 3,71

8.       Mykhalchuk P. K., Bogolubsky A. V., Moroz Y. S., Pipko S. E., Konovets A. I.,Sadkova I. V.,Tolmachev A.
Sulfonyl fluorides as alternative to sulfonyl chlorides in parallel synthesis of aliphatic sulfonamides
ACS Comb. Sci. 2014, 16,192–197.
IF: 3,40

9.       Mykhalchuk P. K., Bogolubsky A. V.; Moroz Y. S.; Granat D. S.; Pipko S. E.; Konovets A. I.; Doroschuk R.; Tolmachev A.
Bis(2,2,2-trifluoroethyl) carbonate as a condensing agent in one-pot, parallel synthesis of unsymmetrical aliphatic ureas
ACS Comb. Sci. 2014, 16,303–308.
IF: 3,40

10.   Mykhalchuk P. K., Bogolubsky A. V.; Moroz Y. S.; Panov, D. M.; Pipko S. E.; Konovets A. I.; Tolmachev A.
A one-pot parallel reductive amination of aldehydes with heteroaromatic amines
ACS Comb. Sci. 2014, 16,375–380.
IF: 3,40

11.   Sholokh M, Zamotaiev OM, Das R, Postupalenko VY, Richert L, Dujardin D, Zaporozhets OA, Pivovarenko VG, Klymchenko AS, Mély Y.
Fluorescent Amino Acid Undergoing Excited State Intramolecular Proton Transfer for Site-Specific Probing and Imaging of Peptide Interactions
J Phys Chem B. 2014 Oct 13.
IF: 3,377

12.   Kucher Olexandr V., Kolodiazhnaya Anastasiya O., Smolii Oleg B., Prisuazhnyk Dmytro V., Tolmacheva Katerina A., Zaporozhets Olga A., Moroz, Yurii S. *,Mykhailiuk Pavel K., Tolmache Andrey A.
Enzyme-Catalyzed Kinetic Resolution of 2,2,2-Trifluoro-1-(heteroaryl)ethanols: Experimental and Docking Studies
European Journal of Organic Chemistry 2014, Issue 34, pages 7692–7698 DOI: 10.1002/ejoc.201403013,
IF: 3,154

13.   Mykhalchuk P. K., Artamonov O., Slobodyanyuk E., Volochnyuk D., Komarov I., Tolmachev A.
Synthesis of trifluoromethyl-substituted 3-azabicyclo[n.1.0]alkanes: advanced building blocks for drug discovery.
J.Org.Chem. 2014, 17, 3592–3598
IF: 3,15

14.   Mykhalchuk P. K., Slobodyanyuk E. Y.,; Artamonov, O. S.; Shishkin, O. V.
One-pot synthesis of CF3-substituted pyrazolines / pyrazoles from electron-deficient alkenes / alkynes and in situ generated CF3CHN2. Optimized synthesis of tris-trifluoromethylpyrazole
J.Org.Chem. 2014, 12, 2487–2495.
IF: 3,15

15.   Tkachenko A. N., Mykhalchuk P. K.,Radchenko S., Babii O., Afonin S., Ulrich A. S., Komarov I. V.
Design and synthesis of a monofluoro-substituted aromatic amino acid as a conformationally restricted 19F-NMR label for membrane-bound peptides.
J.Org.Chem. 2014, 17,3584–3591
IF: 3,15

16.   Mykhalchuk P. K.,Yarmolchuk V. S., Mykhalchuk V. L.
Convenient synthesis of enantiopure (R-) and (S-)-3-fluoro-3-aminomethylpyrrolidines
Tetrahedron 2014, 70, 3011-3017
IF: 2,82

17.   Mykhalchuk P. K., Geraschenko O., Khodakovskiy P., Shishkin O., Tolmachev A.
Synthesis and functionalization of 3-azolyl-quinoxalin-2-ones
Synthesis, 2014, 46, 1487-1492.
IF: 2,50

18.   Mykhalchuk P. K., Yarmoliuk D. V., Arkhipov V. V., Stambirskyi M. V., Dmytriv Y. V., Shishkin O. V., Tolmachev A. A.
Direct Noncatalytic Electrophilic Trifluoroacetylation of Electron-Rich Pyrazoles
Synthesis, 2014, 46, 1254-1260
IF: 2,50

19.   Serdiuk Tetiana, Alekseev Sergei, Lysenko Vladimir, Skryshevsky Valeriy, Géloën Alain
Trypsinization-dependent cell labeling with fluorescent nanoparticles
Nanoscale Research Letters 2014, 9:568, doi:10.1186/1556-276X-9-568
IF: 2,481

20.   Hajjaji H., Alekseev S., Guillot G., Blanchard N.P., Monnier V., Chevolot Y., Brémond G., Querry, M., Philippon D., Vergne, P., Bluet, J.M.
Luminescence nanothermometry with alkyl-capped silicon nanoparticles dispersed in nonpolar liquids
Nanoscale Research Letters, Volume 9, Issue 1, 2014, Pages 1-6.
IF: 2,481

21.   Mykhalchuk P. K., Kucher O. V., Kolodyazhnaya A. O., Smolii O. B., Boiko A. I.,Kubyshkin V. S., Tolmachev A. A.
Enzymatic resolution of chroman-4-ol and its core analogues with Burkholderia cepacia lipase
Tetrahedron Assym. 2014, 25, 563-567.
IF: 2,17

22.   Tsyrulneva I., Zaporozhets O., Piletska E., Piletsky S.
Molecular modelling and synthesis of a polymer for the extraction of amiloride and triamterene from human urin
Anal. Meth. 2014.6. P. 3429-3435.
IF: 1,938

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