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Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface.

Physical review. B, Condensed matter

Borisov AG, Dierkes G, Gauyacq JP, Teillet-Billy D, Winter H.
PMID: 9985852
Phys Rev B Condens Matter. 1996 Dec 15;54(23):17166-17174. doi: 10.1103/physrevb.54.17166.

No abstract available.

Cite
Borisov AG, Dierkes G, Gauyacq JP, et al. Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface. Phys Rev B Condens Matter. 1996;54(23):17166-17174doi: 10.1103/physrevb.54.17166.
Borisov, A. G., Dierkes, G., Gauyacq, J. P., Teillet-Billy, D., & Winter, H. (1996). Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface. Physical review. B, Condensed matter, 54(23), 17166-17174. https://doi.org/10.1103/physrevb.54.17166
Borisov, et al. "Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface." Physical review. B, Condensed matter vol. 54,23 (1996): 17166-17174. doi: https://doi.org/10.1103/physrevb.54.17166
Borisov AG, Dierkes G, Gauyacq JP, Teillet-Billy D, Winter H. Resonant charge transfer in grazing scattering of alkali-metal ions from an Al(111) surface. Phys Rev B Condens Matter. 1996 Dec 15;54(23):17166-17174. doi: 10.1103/physrevb.54.17166. PMID: 9985852.
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High fractions of negative ions in grazing scattering of fast oxygen atoms from a LiF(100) surface.

Physical review letters

Auth C, Borisov AG, Winter H.
PMID: 10059267
Phys Rev Lett. 1995 Sep 18;75(12):2292-2295. doi: 10.1103/PhysRevLett.75.2292.

No abstract available.

Cite
Auth C, Borisov AG, Winter H. High fractions of negative ions in grazing scattering of fast oxygen atoms from a LiF(100) surface. Phys Rev Lett. 1995;75(12):2292-2295doi: 10.1103/PhysRevLett.75.2292.
Auth, C., Borisov, A. G., & Winter, H. (1995). High fractions of negative ions in grazing scattering of fast oxygen atoms from a LiF(100) surface. Physical review letters, 75(12), 2292-2295. https://doi.org/10.1103/PhysRevLett.75.2292
Auth, et al. "High fractions of negative ions in grazing scattering of fast oxygen atoms from a LiF(100) surface." Physical review letters vol. 75,12 (1995): 2292-2295. doi: https://doi.org/10.1103/PhysRevLett.75.2292
Auth C, Borisov AG, Winter H. High fractions of negative ions in grazing scattering of fast oxygen atoms from a LiF(100) surface. Phys Rev Lett. 1995 Sep 18;75(12):2292-2295. doi: 10.1103/PhysRevLett.75.2292. PMID: 10059267.
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Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines.

The Journal of organic chemistry

Novikov RA, Borisov DD, Zotova MA, Denisov DA, Tkachev YV, Korolev VA, Shulishov EV, Tomilov YV.
PMID: 29873492
J Org Chem. 2018 Aug 03;83(15):7836-7851. doi: 10.1021/acs.joc.8b00725. Epub 2018 Jun 22.

A new cascade process for reactions of donor-acceptor cyclopropanes (DACs) with spiro[cyclopropanepyrazolines] in the presence of EtAlCl

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Novikov RA, Borisov DD, Zotova MA, et al. Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines. J Org Chem. 2018;83(15):7836-7851doi: 10.1021/acs.joc.8b00725.
Novikov, R. A., Borisov, D. D., Zotova, M. A., Denisov, D. A., Tkachev, Y. V., Korolev, V. A., Shulishov, E. V., & Tomilov, Y. V. (2018). Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines. The Journal of organic chemistry, 83(15), 7836-7851. https://doi.org/10.1021/acs.joc.8b00725
Novikov, Roman A, et al. "Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines." The Journal of organic chemistry vol. 83,15 (2018): 7836-7851. doi: https://doi.org/10.1021/acs.joc.8b00725
Novikov RA, Borisov DD, Zotova MA, Denisov DA, Tkachev YV, Korolev VA, Shulishov EV, Tomilov YV. Cascade Cleavage of Three-Membered Rings in the Reaction of D-A Cyclopropanes with 4,5-Diazaspiro[2.4]hept-4-enes: A Route to Highly Functionalized Pyrazolines. J Org Chem. 2018 Aug 03;83(15):7836-7851. doi: 10.1021/acs.joc.8b00725. Epub 2018 Jun 22. PMID: 29873492.
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Valproic Acid Increases the Hepatic Differentiation Potential of Salivary Gland Cells.

Acta naturae

Petrakova OS, Ashapkin VV, Shtratnikova VY, Kutueva LI, Vorotelyak EA, Borisov MA, Terskikh VV, Gvazava IG, Vasiliev AV.
PMID: 26798494
Acta Naturae. 2015 Oct-Dec;7(4):80-92.

The studies of cell plasticity and differentiation abilities are important problems in modern cellular biology. The use of histone deacetylase inhibitor - valproic acid is a promising approach to increasing the differentiation efficiency of various cell types. In this...

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Petrakova OS, Ashapkin VV, Shtratnikova VY, et al. Valproic Acid Increases the Hepatic Differentiation Potential of Salivary Gland Cells. Acta Naturae. 2015;7(4):80-92
Petrakova, O. S., Ashapkin, V. V., Shtratnikova, V. Y., Kutueva, L. I., Vorotelyak, E. A., Borisov, M. A., Terskikh, V. V., Gvazava, I. G., & Vasiliev, A. V. (2015). Valproic Acid Increases the Hepatic Differentiation Potential of Salivary Gland Cells. Acta naturae, 7(4), 80-92.
Petrakova, O S, et al. "Valproic Acid Increases the Hepatic Differentiation Potential of Salivary Gland Cells." Acta naturae vol. 7,4 (2015): 80-92.
Petrakova OS, Ashapkin VV, Shtratnikova VY, Kutueva LI, Vorotelyak EA, Borisov MA, Terskikh VV, Gvazava IG, Vasiliev AV. Valproic Acid Increases the Hepatic Differentiation Potential of Salivary Gland Cells. Acta Naturae. 2015 Oct-Dec;7(4):80-92. PMID: 26798494; PMCID: PMC4717252.
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New sources of .

PeerJ

Sulima AS, Zhukov VA, Kulaeva OA, Vasileva EN, Borisov AY, Tikhonovich IA.
PMID: 31768303
PeerJ. 2019 Nov 20;7:e8070. doi: 10.7717/peerj.8070. eCollection 2019.

At the onset of legume-rhizobial symbiosis, the mutual recognition of partners occurs based on a complicated interaction between signal molecules and receptors. Bacterial signal molecules named Nod factors ("nodulation factors") are perceived by the plant LysM-containing receptor-like kinases (LysM-RLKs)...

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Sulima AS, Zhukov VA, Kulaeva OA, et al. New sources of . PeerJ. 2019;7:e8070doi: 10.7717/peerj.8070.
Sulima, A. S., Zhukov, V. A., Kulaeva, O. A., Vasileva, E. N., Borisov, A. Y., & Tikhonovich, I. A. (2019). New sources of . PeerJ, 7e8070. https://doi.org/10.7717/peerj.8070
Sulima, Anton S, et al. "New sources of ." PeerJ vol. 7 (2019): e8070. doi: https://doi.org/10.7717/peerj.8070
Sulima AS, Zhukov VA, Kulaeva OA, Vasileva EN, Borisov AY, Tikhonovich IA. New sources of . PeerJ. 2019 Nov 20;7:e8070. doi: 10.7717/peerj.8070. eCollection 2019. PMID: 31768303; PMCID: PMC6874852.
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Complete negative-ion conversion of halogen atoms and positive ions in surface scattering from KI(100).

Physical review. A, Atomic, molecular, and optical physics

Auth C, Borisov AG, Mertens A, Winter H.
PMID: 9913745
Phys Rev A. 1996 Sep;54(3):2486-2488. doi: 10.1103/physreva.54.2486.

No abstract available.

Cite
Auth C, Borisov AG, Mertens A, et al. Complete negative-ion conversion of halogen atoms and positive ions in surface scattering from KI(100). Phys Rev A. 1996;54(3):2486-2488doi: 10.1103/physreva.54.2486.
Auth, C., Borisov, A. G., Mertens, A., & Winter, H. (1996). Complete negative-ion conversion of halogen atoms and positive ions in surface scattering from KI(100). Physical review. A, Atomic, molecular, and optical physics, 54(3), 2486-2488. https://doi.org/10.1103/physreva.54.2486
Auth, et al. "Complete negative-ion conversion of halogen atoms and positive ions in surface scattering from KI(100)." Physical review. A, Atomic, molecular, and optical physics vol. 54,3 (1996): 2486-2488. doi: https://doi.org/10.1103/physreva.54.2486
Auth C, Borisov AG, Mertens A, Winter H. Complete negative-ion conversion of halogen atoms and positive ions in surface scattering from KI(100). Phys Rev A. 1996 Sep;54(3):2486-2488. doi: 10.1103/physreva.54.2486. PMID: 9913745.
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Bridging quantum and classical plasmonics with a quantum-corrected model.

Nature communications

Esteban R, Borisov AG, Nordlander P, Aizpurua J.
PMID: 22569369
Nat Commun. 2012 May 08;3:825. doi: 10.1038/ncomms1806.

Electromagnetic coupling between plasmonic resonances in metallic nanoparticles allows for engineering of the optical response and generation of strong localized near-fields. Classical electrodynamics fails to describe this coupling across sub-nanometer gaps, where quantum effects become important owing to non-local...

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Esteban R, Borisov AG, Nordlander P, et al. Bridging quantum and classical plasmonics with a quantum-corrected model. Nat Commun. 2012;3:825doi: 10.1038/ncomms1806.
Esteban, R., Borisov, A. G., Nordlander, P., & Aizpurua, J. (2012). Bridging quantum and classical plasmonics with a quantum-corrected model. Nature communications, 3825. https://doi.org/10.1038/ncomms1806
Esteban, Ruben, et al. "Bridging quantum and classical plasmonics with a quantum-corrected model." Nature communications vol. 3 (2012): 825. doi: https://doi.org/10.1038/ncomms1806
Esteban R, Borisov AG, Nordlander P, Aizpurua J. Bridging quantum and classical plasmonics with a quantum-corrected model. Nat Commun. 2012 May 08;3:825. doi: 10.1038/ncomms1806. PMID: 22569369.
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Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor-Acceptor Cyclopropanes.

Angewandte Chemie (International ed. in English)

Novikov RA, Borisov DD, Tarasova AV, Tkachev YV, Tomilov YV.
PMID: 29897640
Angew Chem Int Ed Engl. 2018 Aug 06;57(32):10293-10298. doi: 10.1002/anie.201803541. Epub 2018 Jul 17.

A new strategy for the three-component addition of halide anions and acetylenes to donor-acceptor cyclopropanes (DACs) is presented. This reaction, which occurs with high E selectivity, is promoted by gallium(III) salts and based on the 1,2-zwitterionic reactivity of DACs....

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Novikov RA, Borisov DD, Tarasova AV, et al. Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor-Acceptor Cyclopropanes. Angew Chem Int Ed Engl. 2018;57(32):10293-10298doi: 10.1002/anie.201803541.
Novikov, R. A., Borisov, D. D., Tarasova, A. V., Tkachev, Y. V., & Tomilov, Y. V. (2018). Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor-Acceptor Cyclopropanes. Angewandte Chemie (International ed. in English), 57(32), 10293-10298. https://doi.org/10.1002/anie.201803541
Novikov, Roman A, et al. "Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor-Acceptor Cyclopropanes." Angewandte Chemie (International ed. in English) vol. 57,32 (2018): 10293-10298. doi: https://doi.org/10.1002/anie.201803541
Novikov RA, Borisov DD, Tarasova AV, Tkachev YV, Tomilov YV. Three-Component Gallium(III)-Promoted Addition of Halide Anions and Acetylenes to Donor-Acceptor Cyclopropanes. Angew Chem Int Ed Engl. 2018 Aug 06;57(32):10293-10298. doi: 10.1002/anie.201803541. Epub 2018 Jul 17. PMID: 29897640.
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Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-.

Beilstein journal of organic chemistry

Lipson VV, Pavlovska TL, Svetlichnaya NV, Poryvai AA, Gorobets NY, Van der Eycken EV, Konovalova IS, Shiskina SV, Borisov AV, Musatov VI, Mazepa AV.
PMID: 31164941
Beilstein J Org Chem. 2019 May 06;15:1032-1045. doi: 10.3762/bjoc.15.101. eCollection 2019.

The unexpectedly uncatalyzed reaction between 2-amino-4-arylimidazoles, aromatic aldehydes and Meldrum's acid has selectively led to the corresponding Knoevenagel-Michael adducts containing a free amino group in the imidazole fragment. The adducts derived from Meldrum's acid have been smoothly converted into...

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Lipson VV, Pavlovska TL, Svetlichnaya NV, et al. Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-. Beilstein J Org Chem. 2019;15:1032-1045doi: 10.3762/bjoc.15.101.
Lipson, V. V., Pavlovska, T. L., Svetlichnaya, N. V., Poryvai, A. A., Gorobets, N. Y., Van der Eycken, E. V., Konovalova, I. S., Shiskina, S. V., Borisov, A. V., Musatov, V. I., & Mazepa, A. V. (2019). Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-. Beilstein journal of organic chemistry, 151032-1045. https://doi.org/10.3762/bjoc.15.101
Lipson, Victoria V, et al. "Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-." Beilstein journal of organic chemistry vol. 15 (2019): 1032-1045. doi: https://doi.org/10.3762/bjoc.15.101
Lipson VV, Pavlovska TL, Svetlichnaya NV, Poryvai AA, Gorobets NY, Van der Eycken EV, Konovalova IS, Shiskina SV, Borisov AV, Musatov VI, Mazepa AV. Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-. Beilstein J Org Chem. 2019 May 06;15:1032-1045. doi: 10.3762/bjoc.15.101. eCollection 2019. PMID: 31164941; PMCID: PMC6541323.
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Correction: Novel cationic 1,2,4-selenadiazoles: synthesis .

Dalton transactions (Cambridge, England : 2003)

Khrustalev VN, Grishina MM, Matsulevich ZV, Lukiyanova JM, Borisova GN, Osmanov VK, Novikov AS, Kirichuk AA, Borisov AV, Solari E, Tskhovrebov AG.
PMID: 34494059
Dalton Trans. 2021 Sep 21;50(36):12730. doi: 10.1039/d1dt90151f.

Correction for 'Novel cationic 1,2,4-selenadiazoles: synthesis

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Khrustalev VN, Grishina MM, Matsulevich ZV, et al. Correction: Novel cationic 1,2,4-selenadiazoles: synthesis . Dalton Trans. 2021;50(36):12730doi: 10.1039/d1dt90151f.
Khrustalev, V. N., Grishina, M. M., Matsulevich, Z. V., Lukiyanova, J. M., Borisova, G. N., Osmanov, V. K., Novikov, A. S., Kirichuk, A. A., Borisov, A. V., Solari, E., & Tskhovrebov, A. G. (2021). Correction: Novel cationic 1,2,4-selenadiazoles: synthesis . Dalton transactions (Cambridge, England : 2003), 50(36), 12730. https://doi.org/10.1039/d1dt90151f
Khrustalev, Victor N, et al. "Correction: Novel cationic 1,2,4-selenadiazoles: synthesis ." Dalton transactions (Cambridge, England : 2003) vol. 50,36 (2021): 12730. doi: https://doi.org/10.1039/d1dt90151f
Khrustalev VN, Grishina MM, Matsulevich ZV, Lukiyanova JM, Borisova GN, Osmanov VK, Novikov AS, Kirichuk AA, Borisov AV, Solari E, Tskhovrebov AG. Correction: Novel cationic 1,2,4-selenadiazoles: synthesis . Dalton Trans. 2021 Sep 21;50(36):12730. doi: 10.1039/d1dt90151f. PMID: 34494059.
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1-Year COMBO stent outcomes stratified by the PARIS bleeding prediction score: From the MASCOT registry.

International journal of cardiology. Heart & vasculature

Chandrasekhar J, Baber U, Sartori S, Aquino MB, Hájek P, Atzev B, Hudec M, Kiam Ong T, Mates M, Borisov B, Warda HM, den Heijer P, Wojcik J, Iniguez A, Coufal Z, Khashaba A, Munawar M, Gerber RT, Yan BP, Tejedor P, Kala P, Bang Liew H, Lee M, Kalkman DN, Dangas GD, de Winter RJ, Colombo A, Mehran R.
PMID: 32953969
Int J Cardiol Heart Vasc. 2020 Sep 06;31:100605. doi: 10.1016/j.ijcha.2020.100605. eCollection 2020 Dec.

BACKGROUND: The COMBO stent is a biodegradable-polymer sirolimus-eluting stent with endothelial progenitor cell capture technology for faster endothelialization.OBJECTIVE: We analyzed COMBO stent outcomes in relation to bleeding risk using the PARIS bleeding score.METHODS: MASCOT was an international registry of...

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Chandrasekhar J, Baber U, Sartori S, et al. 1-Year COMBO stent outcomes stratified by the PARIS bleeding prediction score: From the MASCOT registry. Int J Cardiol Heart Vasc. 2020;31:100605doi: 10.1016/j.ijcha.2020.100605.
Chandrasekhar, J., Baber, U., Sartori, S., Aquino, M. B., Hájek, P., Atzev, B., Hudec, M., Kiam Ong, T., Mates, M., Borisov, B., Warda, H. M., den Heijer, P., Wojcik, J., Iniguez, A., Coufal, Z., Khashaba, A., Munawar, M., Gerber, R. T., Yan, B. P., Tejedor, P., Kala, P., Bang Liew, H., Lee, M., Kalkman, D. N., Dangas, G. D., de Winter, R. J., Colombo, A., Mehran, R. (2020). 1-Year COMBO stent outcomes stratified by the PARIS bleeding prediction score: From the MASCOT registry. International journal of cardiology. Heart & vasculature, 31100605. https://doi.org/10.1016/j.ijcha.2020.100605
Chandrasekhar, Jaya, et al. "1-Year COMBO stent outcomes stratified by the PARIS bleeding prediction score: From the MASCOT registry." International journal of cardiology. Heart & vasculature vol. 31 (2020): 100605. doi: https://doi.org/10.1016/j.ijcha.2020.100605
Chandrasekhar J, Baber U, Sartori S, Aquino MB, Hájek P, Atzev B, Hudec M, Kiam Ong T, Mates M, Borisov B, Warda HM, den Heijer P, Wojcik J, Iniguez A, Coufal Z, Khashaba A, Munawar M, Gerber RT, Yan BP, Tejedor P, Kala P, Bang Liew H, Lee M, Kalkman DN, Dangas GD, de Winter RJ, Colombo A, Mehran R. 1-Year COMBO stent outcomes stratified by the PARIS bleeding prediction score: From the MASCOT registry. Int J Cardiol Heart Vasc. 2020 Sep 06;31:100605. doi: 10.1016/j.ijcha.2020.100605. eCollection 2020 Dec. PMID: 32953969; PMCID: PMC7486438.
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Solid Solutions Rb.

Inorganic chemistry

Fukina DG, Suleimanov EV, Boryakov AV, Zubkov SY, Usanov DA, Borisov EV, Lyakaev DV, Fomina LD.
PMID: 32921043
Inorg Chem. 2020 Oct 05;59(19):14118-14133. doi: 10.1021/acs.inorgchem.0c01895. Epub 2020 Sep 13.

Solid solutions Rb

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Fukina DG, Suleimanov EV, Boryakov AV, et al. Solid Solutions Rb. Inorg Chem. 2020;59(19):14118-14133doi: 10.1021/acs.inorgchem.0c01895.
Fukina, D. G., Suleimanov, E. V., Boryakov, A. V., Zubkov, S. Y., Usanov, D. A., Borisov, E. V., Lyakaev, D. V., & Fomina, L. D. (2020). Solid Solutions Rb. Inorganic chemistry, 59(19), 14118-14133. https://doi.org/10.1021/acs.inorgchem.0c01895
Fukina, Diana G, et al. "Solid Solutions Rb." Inorganic chemistry vol. 59,19 (2020): 14118-14133. doi: https://doi.org/10.1021/acs.inorgchem.0c01895
Fukina DG, Suleimanov EV, Boryakov AV, Zubkov SY, Usanov DA, Borisov EV, Lyakaev DV, Fomina LD. Solid Solutions Rb. Inorg Chem. 2020 Oct 05;59(19):14118-14133. doi: 10.1021/acs.inorgchem.0c01895. Epub 2020 Sep 13. PMID: 32921043.
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Showing 13 to 24 of 116 entries