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Dexamethasone attenuates the modulatory effect of the insular cortex on the baroreflex in anesthetized rat.

Canadian journal of physiology and pharmacology

Tumanova TS, Кokurina TN, Rybakova GI, Aleksandrov VG.
PMID: 34644509
Can J Physiol Pharmacol. 2021 Oct 13; doi: 10.1139/cjpp-2021-0385. Epub 2021 Oct 13.

The arterial baroreflex (BR) is an important neural mechanism for the stabilization of arterial pressure (AP). It is known that the insular cortex (IC) and other parts of the central autonomic network (CAN) are able to modulate the BR...

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Tumanova TS, Кokurina TN, Rybakova GI, et al. Dexamethasone attenuates the modulatory effect of the insular cortex on the baroreflex in anesthetized rat. Can J Physiol Pharmacol. 2021;doi: 10.1139/cjpp-2021-0385.
Tumanova, T. S., Кokurina, T. N., Rybakova, G. I., & Aleksandrov, V. G. (2021). Dexamethasone attenuates the modulatory effect of the insular cortex on the baroreflex in anesthetized rat. Canadian journal of physiology and pharmacology, . https://doi.org/10.1139/cjpp-2021-0385
Tumanova, Tatiana Sergeevna, et al. "Dexamethasone attenuates the modulatory effect of the insular cortex on the baroreflex in anesthetized rat." Canadian journal of physiology and pharmacology vol. (2021). doi: https://doi.org/10.1139/cjpp-2021-0385
Tumanova TS, Кokurina TN, Rybakova GI, Aleksandrov VG. Dexamethasone attenuates the modulatory effect of the insular cortex on the baroreflex in anesthetized rat. Can J Physiol Pharmacol. 2021 Oct 13; doi: 10.1139/cjpp-2021-0385. Epub 2021 Oct 13. PMID: 34644509.
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Expanding Stereoelectronic Limits of .

Journal of the American Chemical Society

Vartanova AE, Plodukhin AY, Ratmanova NK, Andreev IA, Anisimov MN, Gudimchuk NB, Rybakov VB, Levina II, Ivanova OA, Trushkov IV, Alabugin IV.
PMID: 34406759
J Am Chem Soc. 2021 Sep 01;143(34):13952-13961. doi: 10.1021/jacs.1c07088. Epub 2021 Aug 18.

The importance of intramolecular constraints in cyclic transition-state geometries is especially pronounced in

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Vartanova AE, Plodukhin AY, Ratmanova NK, et al. Expanding Stereoelectronic Limits of . J Am Chem Soc. 2021;143(34):13952-13961doi: 10.1021/jacs.1c07088.
Vartanova, A. E., Plodukhin, A. Y., Ratmanova, N. K., Andreev, I. A., Anisimov, M. N., Gudimchuk, N. B., Rybakov, V. B., Levina, I. I., Ivanova, O. A., Trushkov, I. V., & Alabugin, I. V. (2021). Expanding Stereoelectronic Limits of . Journal of the American Chemical Society, 143(34), 13952-13961. https://doi.org/10.1021/jacs.1c07088
Vartanova, Anna E, et al. "Expanding Stereoelectronic Limits of ." Journal of the American Chemical Society vol. 143,34 (2021): 13952-13961. doi: https://doi.org/10.1021/jacs.1c07088
Vartanova AE, Plodukhin AY, Ratmanova NK, Andreev IA, Anisimov MN, Gudimchuk NB, Rybakov VB, Levina II, Ivanova OA, Trushkov IV, Alabugin IV. Expanding Stereoelectronic Limits of . J Am Chem Soc. 2021 Sep 01;143(34):13952-13961. doi: 10.1021/jacs.1c07088. Epub 2021 Aug 18. PMID: 34406759.
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Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group.

Organic letters

Ivanova OA, Andronov VA, Vasin VS, Shumsky AN, Rybakov VB, Voskressensky LG, Trushkov IV.
PMID: 30517005
Org Lett. 2018 Dec 21;20(24):7947-7952. doi: 10.1021/acs.orglett.8b03491. Epub 2018 Dec 05.

Lewis-acid-induced domino transformations of donor-acceptor cyclopropanes, possessing a nucleophilic center embedded in a donor group, into functionalized 2,3-dihydrobenzo[ b]furans and 2,3-dihydrobenzo[ b]thiophenes are reported herein. An unusual switch of the electrophilic center in the three-membered ring, from the atom...

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Ivanova OA, Andronov VA, Vasin VS, et al. Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group. Org Lett. 2018;20(24):7947-7952doi: 10.1021/acs.orglett.8b03491.
Ivanova, O. A., Andronov, V. A., Vasin, V. S., Shumsky, A. N., Rybakov, V. B., Voskressensky, L. G., & Trushkov, I. V. (2018). Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group. Organic letters, 20(24), 7947-7952. https://doi.org/10.1021/acs.orglett.8b03491
Ivanova, Olga A, et al. "Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group." Organic letters vol. 20,24 (2018): 7947-7952. doi: https://doi.org/10.1021/acs.orglett.8b03491
Ivanova OA, Andronov VA, Vasin VS, Shumsky AN, Rybakov VB, Voskressensky LG, Trushkov IV. Expanding the Reactivity of Donor-Acceptor Cyclopropanes: Synthesis of Benzannulated Five-Membered Heterocycles via Intramolecular Attack of a Pendant Nucleophilic Group. Org Lett. 2018 Dec 21;20(24):7947-7952. doi: 10.1021/acs.orglett.8b03491. Epub 2018 Dec 05. PMID: 30517005.
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(2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate.

Acta crystallographica. Section E, Structure reports online

Kurkin AV, Bernovskaya AA, Yurovskaya MA, Rybakov VB.
PMID: 21203163
Acta Crystallogr Sect E Struct Rep Online. 2008 Jul 09;64:o1448. doi: 10.1107/S1600536808020588.

The title compound, C(13)H(12)BrNO(4), was obtained from an optically active aniline derivative. The structure was characterized by (1)H NMR, (13)C NMR, MS and X-ray diffraction techniques. 86% of the atoms of the two independent mol-ecules in the asymmetric unit...

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Kurkin AV, Bernovskaya AA, Yurovskaya MA, et al. (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate. Acta Crystallogr Sect E Struct Rep Online. 2008;64:o1448doi: 10.1107/S1600536808020588.
Kurkin, A. V., Bernovskaya, A. A., Yurovskaya, M. A., & Rybakov, V. B. (2008). (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate. Acta crystallographica. Section E, Structure reports online, 64o1448. https://doi.org/10.1107/S1600536808020588
Kurkin, Alexander V, et al. "(2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate." Acta crystallographica. Section E, Structure reports online vol. 64 (2008): o1448. doi: https://doi.org/10.1107/S1600536808020588
Kurkin AV, Bernovskaya AA, Yurovskaya MA, Rybakov VB. (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate. Acta Crystallogr Sect E Struct Rep Online. 2008 Jul 09;64:o1448. doi: 10.1107/S1600536808020588. PMID: 21203163; PMCID: PMC2961954.
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meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(III) complexes: synthesis, structure, spectral properties and electrochemistry.

Dalton transactions (Cambridge, England : 2003)

Pushkarev VE, Kalashnikov VV, Tolbin AY, Trashin SA, Borisova NE, Simonov SV, Rybakov VB, Tomilova LG, Zefirov NS.
PMID: 26332086
Dalton Trans. 2015 Oct 07;44(37):16553-64. doi: 10.1039/c5dt01933h.

A series of half-sandwich and sandwich-type lanthanide(III) complexes have been prepared using tetrabenzotriazaporphyrin ligands. Reaction of 27-phenyl-29H,31H-tetrabenzo[b,g,l,q][5,10,15]-triazaporphyrin (PhTBTAPH2, 1) with salts [LnX3]·nH2O (Ln = Eu (a), Lu (b); X = OAc, acac) afforded the single- and homoleptic double-deckers (PhTBTAP)LnOAc...

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Pushkarev VE, Kalashnikov VV, Tolbin AY, et al. meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(III) complexes: synthesis, structure, spectral properties and electrochemistry. Dalton Trans. 2015;44(37):16553-64doi: 10.1039/c5dt01933h.
Pushkarev, V. E., Kalashnikov, V. V., Tolbin, A. Y., Trashin, S. A., Borisova, N. E., Simonov, S. V., Rybakov, V. B., Tomilova, L. G., & Zefirov, N. S. (2015). meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(III) complexes: synthesis, structure, spectral properties and electrochemistry. Dalton transactions (Cambridge, England : 2003), 44(37), 16553-64. https://doi.org/10.1039/c5dt01933h
Pushkarev, Victor E, et al. "meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(III) complexes: synthesis, structure, spectral properties and electrochemistry." Dalton transactions (Cambridge, England : 2003) vol. 44,37 (2015): 16553-64. doi: https://doi.org/10.1039/c5dt01933h
Pushkarev VE, Kalashnikov VV, Tolbin AY, Trashin SA, Borisova NE, Simonov SV, Rybakov VB, Tomilova LG, Zefirov NS. meso-Phenyltetrabenzotriazaporphyrin based double-decker lanthanide(III) complexes: synthesis, structure, spectral properties and electrochemistry. Dalton Trans. 2015 Oct 07;44(37):16553-64. doi: 10.1039/c5dt01933h. PMID: 26332086.
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Convenient access to pyrrolidin-3-ylphosphonic acids and tetrahydro-2.

Beilstein journal of organic chemistry

Reznikov AN, Nikerov DS, Sibiryakova AE, Rybakov VB, Golovin EV, Klimochkin YN.
PMID: 32952723
Beilstein J Org Chem. 2020 Aug 25;16:2073-2079. doi: 10.3762/bjoc.16.174. eCollection 2020.

A new synthetic strategy toward nonracemic phosphoryl-substituted pyrrolidines and tetrahydropyranes with three and five contiguous stereocenters is presented. Readily available β-keto phosphonates react with conjugated nitroolefins in the presence of a chiral Ni(II) complex to give nitro keto phosphonates...

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Reznikov AN, Nikerov DS, Sibiryakova AE, et al. Convenient access to pyrrolidin-3-ylphosphonic acids and tetrahydro-2. Beilstein J Org Chem. 2020;16:2073-2079doi: 10.3762/bjoc.16.174.
Reznikov, A. N., Nikerov, D. S., Sibiryakova, A. E., Rybakov, V. B., Golovin, E. V., & Klimochkin, Y. N. (2020). Convenient access to pyrrolidin-3-ylphosphonic acids and tetrahydro-2. Beilstein journal of organic chemistry, 162073-2079. https://doi.org/10.3762/bjoc.16.174
Reznikov, Alexander N, et al. "Convenient access to pyrrolidin-3-ylphosphonic acids and tetrahydro-2." Beilstein journal of organic chemistry vol. 16 (2020): 2073-2079. doi: https://doi.org/10.3762/bjoc.16.174
Reznikov AN, Nikerov DS, Sibiryakova AE, Rybakov VB, Golovin EV, Klimochkin YN. Convenient access to pyrrolidin-3-ylphosphonic acids and tetrahydro-2. Beilstein J Org Chem. 2020 Aug 25;16:2073-2079. doi: 10.3762/bjoc.16.174. eCollection 2020. PMID: 32952723; PMCID: PMC7476589.
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External Ventricular Drainage Complication Risks and Accuracy Analysis.

World neurosurgery

Konovalov AN, Grebenev FV, Rybakov VA, Pilipenko YV, Shekhtman OD, Okishev DN, Yershova ON, Eliava SS.
PMID: 34543732
World Neurosurg. 2021 Dec;156:e276-e282. doi: 10.1016/j.wneu.2021.09.051. Epub 2021 Sep 20.

OBJECTIVE: The setting of external ventricular drainage (EVD) is one of the most frequent procedures in the neurosurgical practice. However, complication risks of this procedure may grow from 5% to 39%. The number of publications concerning the advancement of...

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Konovalov AN, Grebenev FV, Rybakov VA, et al. External Ventricular Drainage Complication Risks and Accuracy Analysis. World Neurosurg. 2021;156:e276-e282doi: 10.1016/j.wneu.2021.09.051.
Konovalov, A. N., Grebenev, F. V., Rybakov, V. A., Pilipenko, Y. V., Shekhtman, O. D., Okishev, D. N., Yershova, O. N., & Eliava, S. S. (2021). External Ventricular Drainage Complication Risks and Accuracy Analysis. World neurosurgery, 156e276-e282. https://doi.org/10.1016/j.wneu.2021.09.051
Konovalov, Anton Nikolaevich, et al. "External Ventricular Drainage Complication Risks and Accuracy Analysis." World neurosurgery vol. 156 (2021): e276-e282. doi: https://doi.org/10.1016/j.wneu.2021.09.051
Konovalov AN, Grebenev FV, Rybakov VA, Pilipenko YV, Shekhtman OD, Okishev DN, Yershova ON, Eliava SS. External Ventricular Drainage Complication Risks and Accuracy Analysis. World Neurosurg. 2021 Dec;156:e276-e282. doi: 10.1016/j.wneu.2021.09.051. Epub 2021 Sep 20. PMID: 34543732.
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Wagner-Meerwein type rearrangement in 5-oxohomoadamantane series.

Organic & biomolecular chemistry

Tkachenko IM, Mankova PA, Rybakov VB, Golovin EV, Klimochkin YN.
PMID: 31845947
Org Biomol Chem. 2020 Jan 22;18(3):465-478. doi: 10.1039/c9ob02060h.

Efficient methods for introducing various substituents into the α-position of ethyl 5-oxohomoadamantyl-4-carboxylate are reported. An unexpected acid-catalysed 1,2-alkyl shift in the series of synthesized α,α-bis-substituted 5-oxohomoadamantanes, and also in the hydroxy derivatives of homoadamantane was found. Such a retropinacol-like...

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Tkachenko IM, Mankova PA, Rybakov VB, et al. Wagner-Meerwein type rearrangement in 5-oxohomoadamantane series. Org Biomol Chem. 2020;18(3):465-478doi: 10.1039/c9ob02060h.
Tkachenko, I. M., Mankova, P. A., Rybakov, V. B., Golovin, E. V., & Klimochkin, Y. N. (2020). Wagner-Meerwein type rearrangement in 5-oxohomoadamantane series. Organic & biomolecular chemistry, 18(3), 465-478. https://doi.org/10.1039/c9ob02060h
Tkachenko, Ilya M, et al. "Wagner-Meerwein type rearrangement in 5-oxohomoadamantane series." Organic & biomolecular chemistry vol. 18,3 (2020): 465-478. doi: https://doi.org/10.1039/c9ob02060h
Tkachenko IM, Mankova PA, Rybakov VB, Golovin EV, Klimochkin YN. Wagner-Meerwein type rearrangement in 5-oxohomoadamantane series. Org Biomol Chem. 2020 Jan 22;18(3):465-478. doi: 10.1039/c9ob02060h. PMID: 31845947.
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Photoredox-Catalyzed Hydrosulfonylation of Arylallenes.

The Journal of organic chemistry

Storozhenko OA, Festa AA, Detistova GI, Rybakov VB, Varlamov AV, Van der Eycken EV, Voskressensky LG.
PMID: 31874037
J Org Chem. 2020 Feb 21;85(4):2250-2259. doi: 10.1021/acs.joc.9b02960. Epub 2020 Jan 06.

(Het)Arylallenes undergo hydrosulfonylation under photoredox-catalyzed conditions. The reaction gives vinyl sulfones in a regio- and diastereoselective manner, employing sodium sulfinates as the sulfonyl source and eosin Y as the photocatalyst. Indol-1-yl, pyrrol-1-yl, phenyl, and naphtylallenes might be used. Aliphatic...

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Storozhenko OA, Festa AA, Detistova GI, et al. Photoredox-Catalyzed Hydrosulfonylation of Arylallenes. J Org Chem. 2020;85(4):2250-2259doi: 10.1021/acs.joc.9b02960.
Storozhenko, O. A., Festa, A. A., Detistova, G. I., Rybakov, V. B., Varlamov, A. V., Van der Eycken, E. V., & Voskressensky, L. G. (2020). Photoredox-Catalyzed Hydrosulfonylation of Arylallenes. The Journal of organic chemistry, 85(4), 2250-2259. https://doi.org/10.1021/acs.joc.9b02960
Storozhenko, Olga A, et al. "Photoredox-Catalyzed Hydrosulfonylation of Arylallenes." The Journal of organic chemistry vol. 85,4 (2020): 2250-2259. doi: https://doi.org/10.1021/acs.joc.9b02960
Storozhenko OA, Festa AA, Detistova GI, Rybakov VB, Varlamov AV, Van der Eycken EV, Voskressensky LG. Photoredox-Catalyzed Hydrosulfonylation of Arylallenes. J Org Chem. 2020 Feb 21;85(4):2250-2259. doi: 10.1021/acs.joc.9b02960. Epub 2020 Jan 06. PMID: 31874037.
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A Facile Approach to Bis(isoxazoles), Promising Ligands of the AMPA Receptor.

Molecules (Basel, Switzerland)

Vasilenko DA, Sadovnikov KS, Sedenkova KN, Karlov DS, Radchenko EV, Grishin YK, Rybakov VB, Kuznetsova TS, Zamoyski VL, Grigoriev VV, Palyulin VA, Averina EB.
PMID: 34770819
Molecules. 2021 Oct 23;26(21). doi: 10.3390/molecules26216411.

A convenient synthetic approach to novel functionalized bis(isoxazoles), the promising bivalent ligands of the AMPA receptor, was elaborated. It was based on the heterocyclization reactions of readily available electrophilic alkenes with the tetranitromethane-triethylamine complex. The structural diversity of the...

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Vasilenko DA, Sadovnikov KS, Sedenkova KN, et al. A Facile Approach to Bis(isoxazoles), Promising Ligands of the AMPA Receptor. Molecules. 2021;26(21)doi: 10.3390/molecules26216411.
Vasilenko, D. A., Sadovnikov, K. S., Sedenkova, K. N., Karlov, D. S., Radchenko, E. V., Grishin, Y. K., Rybakov, V. B., Kuznetsova, T. S., Zamoyski, V. L., Grigoriev, V. V., Palyulin, V. A., & Averina, E. B. (2021). A Facile Approach to Bis(isoxazoles), Promising Ligands of the AMPA Receptor. Molecules (Basel, Switzerland), 26(21), . https://doi.org/10.3390/molecules26216411
Vasilenko, Dmitry A, et al. "A Facile Approach to Bis(isoxazoles), Promising Ligands of the AMPA Receptor." Molecules (Basel, Switzerland) vol. 26,21 (2021). doi: https://doi.org/10.3390/molecules26216411
Vasilenko DA, Sadovnikov KS, Sedenkova KN, Karlov DS, Radchenko EV, Grishin YK, Rybakov VB, Kuznetsova TS, Zamoyski VL, Grigoriev VV, Palyulin VA, Averina EB. A Facile Approach to Bis(isoxazoles), Promising Ligands of the AMPA Receptor. Molecules. 2021 Oct 23;26(21). doi: 10.3390/molecules26216411. PMID: 34770819; PMCID: PMC8588558.
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5-Nitroisoxazoles in S.

Organic & biomolecular chemistry

Vasilenko DA, Dronov SE, Parfiryeu DU, Sadovnikov KS, Sedenkova KN, Grishin YK, Rybakov VB, Kuznetsova TS, Averina EB.
PMID: 34236067
Org Biomol Chem. 2021 Jul 28;19(29):6447-6454. doi: 10.1039/d1ob00816a.

An efficient protocol for the straightforward functionalization of the isoxazole ring via the reactions of aromatic nucleophilic substitution of the nitro group with various nucleophiles has been elaborated. The method features excellent chemical yields, easy operability of the reaction,...

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Vasilenko DA, Dronov SE, Parfiryeu DU, et al. 5-Nitroisoxazoles in S. Org Biomol Chem. 2021;19(29):6447-6454doi: 10.1039/d1ob00816a.
Vasilenko, D. A., Dronov, S. E., Parfiryeu, D. U., Sadovnikov, K. S., Sedenkova, K. N., Grishin, Y. K., Rybakov, V. B., Kuznetsova, T. S., & Averina, E. B. (2021). 5-Nitroisoxazoles in S. Organic & biomolecular chemistry, 19(29), 6447-6454. https://doi.org/10.1039/d1ob00816a
Vasilenko, Dmitry A, et al. "5-Nitroisoxazoles in S." Organic & biomolecular chemistry vol. 19,29 (2021): 6447-6454. doi: https://doi.org/10.1039/d1ob00816a
Vasilenko DA, Dronov SE, Parfiryeu DU, Sadovnikov KS, Sedenkova KN, Grishin YK, Rybakov VB, Kuznetsova TS, Averina EB. 5-Nitroisoxazoles in S. Org Biomol Chem. 2021 Jul 28;19(29):6447-6454. doi: 10.1039/d1ob00816a. PMID: 34236067.
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Expanding Stereoelectronic Limits of .

Journal of the American Chemical Society

Vartanova AE, Plodukhin AY, Ratmanova NK, Andreev IA, Anisimov MN, Gudimchuk NB, Rybakov VB, Levina II, Ivanova OA, Trushkov IV, Alabugin IV.
PMID: 34406759
J Am Chem Soc. 2021 Sep 01;143(34):13952-13961. doi: 10.1021/jacs.1c07088. Epub 2021 Aug 18.

The importance of intramolecular constraints in cyclic transition-state geometries is especially pronounced in

Cite
Vartanova AE, Plodukhin AY, Ratmanova NK, et al. Expanding Stereoelectronic Limits of . J Am Chem Soc. 2021;143(34):13952-13961doi: 10.1021/jacs.1c07088.
Vartanova, A. E., Plodukhin, A. Y., Ratmanova, N. K., Andreev, I. A., Anisimov, M. N., Gudimchuk, N. B., Rybakov, V. B., Levina, I. I., Ivanova, O. A., Trushkov, I. V., & Alabugin, I. V. (2021). Expanding Stereoelectronic Limits of . Journal of the American Chemical Society, 143(34), 13952-13961. https://doi.org/10.1021/jacs.1c07088
Vartanova, Anna E, et al. "Expanding Stereoelectronic Limits of ." Journal of the American Chemical Society vol. 143,34 (2021): 13952-13961. doi: https://doi.org/10.1021/jacs.1c07088
Vartanova AE, Plodukhin AY, Ratmanova NK, Andreev IA, Anisimov MN, Gudimchuk NB, Rybakov VB, Levina II, Ivanova OA, Trushkov IV, Alabugin IV. Expanding Stereoelectronic Limits of . J Am Chem Soc. 2021 Sep 01;143(34):13952-13961. doi: 10.1021/jacs.1c07088. Epub 2021 Aug 18. PMID: 34406759.
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Showing 13 to 24 of 61 entries