Works matching AU Rakitin, Oleg A.
Results: 82
Effective synthesis of 4,5-dibromobenzo[1,2-c:3,4-c']-bis([1,2,5]thiadiazole) by bromination of benzo[1,2-c:3,4-c']-bis([1,2,5]thiadiazole).
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 7/8, p. 403, doi. 10.1007/s10593-024-03352-w
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Cyclopent-4-ene-1,3-diones fused with heterocycles as promising anchor groups in non-fullerene acceptors (microreview).
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- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 3/4, p. 127, doi. 10.1007/s10593-024-03306-2
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Benzobischalcogenadiazoles: synthesis and applications (microreview).
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- Chemistry of Heterocyclic Compounds, 2022, v. 58, n. 6/7, p. 307, doi. 10.1007/s10593-022-03088-5
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Synthesis of Sulfur-Containing Heterocycles by Electrophilic Addition Reactions of Disulfur Dichloride.
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- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 7, p. 837, doi. 10.1007/s10593-020-02740-2
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Furoxans fused with heterocycles as promising donors and precursors for nitric oxide donors (microreview).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 8, p. 849, doi. 10.1007/s10593-017-2135-4
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4,7-Dibromo-substituted 2,1,3-benzothia(selena,oxa)diazoles and [1, 2, 5]thia(selena)diazolo[3,4- c]pyridines as building blocks in solar cells components (microreview).
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 8, p. 855, doi. 10.1007/s10593-017-2137-2
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Suzuki cross-coupling reactions of 4,7-dibromo[1, 2, 5]selenadiazolo[3,4- c]pyridine - a path to new solar cell components.
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- Chemistry of Heterocyclic Compounds, 2017, v. 53, n. 5, p. 608, doi. 10.1007/s10593-017-2099-4
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A short and safe method for the synthesis of [1,2,5]oxadiazolo[3,4- c] pyridine.
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- Chemistry of Heterocyclic Compounds, 2015, v. 51, n. 2, p. 203, doi. 10.1007/s10593-015-1683-8
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A rare case of brominated small molecule acceptors for high-efficiency organic solar cells.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40423-6
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Synthesis of 6,7‐Dihydropyrrolo[2,1‐c][1,3]thiazino[3,2‐a]pyrazine‐4(11bH)‐(thi)ones from 1,2‐Dithiolo‐3‐(thi)ones.
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- European Journal of Organic Chemistry, 2019, v. 2019, n. 26, p. 4149, doi. 10.1002/ejoc.201900142
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Synthesis of the 4,7‐Dibromo Derivative of Highly Electron‐Deficient [1,2,5]Thiadiazolo[3,4‐d]pyridazine and Its Cross‐Coupling Reactions.
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- European Journal of Organic Chemistry, 2018, v. 2018, n. 41, p. 5668, doi. 10.1002/ejoc.201800961
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[1,2,5]Selenadiazolo[3,4- b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selenadiazole and Generation of Persistent Radical Anions.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 25, p. 5585, doi. 10.1002/ejoc.201500742
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Antimicrobial and Antifungal Activity of Rare Substituted 1,2,3-Thiaselenazoles and Corresponding Matched Pair 1,2,3-Dithiazoles.
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- Antibiotics (2079-6382), 2020, v. 9, n. 7, p. 369, doi. 10.3390/antibiotics9070369
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Synthesis and Identification of Pentathiepin-Based Inhibitors of Sporothrix brasiliensis.
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- Antibiotics (2079-6382), 2019, v. 8, n. 4, p. 249, doi. 10.3390/antibiotics8040249
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1,2,5-Chalcogenadiazole-Annulated Tripyrazinoporphyrazines: Synthesis, Spectral Characteristics, and Influence of the Heavy Atom Effect on Their Photophysical Properties.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 3, p. 596, doi. 10.1002/ejoc.201403329
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Breaking the Mold of Discotic Liquid Crystals.
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- Angewandte Chemie International Edition, 1998, v. 37, n. 3, p. 296, doi. 10.1002/(SICI)1521-3773(19980216)37:3<296::AID-ANIE296>3.0.CO;2-U
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From Hünig's Base to Bis([1,2]dithiolo)-[1,4]thiazines in One Pot: The Fast Route to Highly Sulfurated Heterocycles.
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- Angewandte Chemie International Edition, 1997, v. 36, n. 3, p. 281, doi. 10.1002/anie.199702811
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New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction.
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- Chemistry - A European Journal, 2017, v. 23, n. 4, p. 852, doi. 10.1002/chem.201604121
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Synthesis and Physicochemical Properties of 2,7-Disubstituted Phenanthro[2,1-b:7,8-b']dithiophenes.
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- Molecules, 2020, v. 25, n. 17, p. 3842, doi. 10.3390/molecules25173842
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Synthesis of 2-((2-(Benzo[d]oxazol-2-yl)-2H-imidazol-4-yl)amino)-phenols from 2-((5H-1,2,3-Dithiazol-5-ylidene)amino)phenols through Unprecedented Formation of Imidazole Ring from Two Methanimino Groups.
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- Molecules, 2020, v. 25, n. 17, p. 3768, doi. 10.3390/molecules25173768
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Natural Compounds and Their Structural Analogs in Regio- and Stereoselective Synthesis of New Families of Water-Soluble 2H,3H-[1,3]thia- and -Selenazolo[3,2-a]pyridin-4-ium Heterocycles by Annulation Reactions.
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- Molecules, 2020, v. 25, n. 2, p. 376, doi. 10.3390/molecules25020376
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[1,2,5]Thiadiazolo[3,4-d]Pyridazine as an Internal Acceptor in the D-A-π-A Organic Sensitizers for Dye-Sensitized Solar Cells.
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- Molecules, 2019, v. 24, n. 8, p. 1588, doi. 10.3390/molecules24081588
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Safe Synthesis of 4,7-Dibromo[1,2,5]thiadiazolo[3,4-d]pyridazine and Its SNAr Reactions.
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- Molecules, 2018, v. 23, n. 10, p. 2576, doi. 10.3390/molecules23102576
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The Conversion of 5,5′-Bi(1,2,3-dithiazolylidenes) into Isothiazolo[5,4-d]isothiazoles.
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- Molecules, 2018, v. 23, n. 6, p. 1257, doi. 10.3390/molecules23061257
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Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
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- Molecules, 2016, v. 21, n. 5, p. 596, doi. 10.3390/molecules21050596
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Direct Exchange of Oxygen and Selenium Atoms in the 1,2,5-Oxadiazoles and 1,2,5-Selenadiazoles by Action of Sulfur Monochloride.
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- Molecules, 2015, v. 20, n. 8, p. 14522, doi. 10.3390/molecules200814522
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Breathing Some New Life into an Old Topic: Chalcogen-Nitrogen π-Heterocycles as Electron Acceptors.
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- Molecules, 2013, v. 18, n. 8, p. 9850, doi. 10.3390/molecules18089850
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Investigation of the Pentathiepin Functionality as an Inhibitor of Feline Immunodeficiency Virus (FIV) via a Potential Zinc Ejection Mechanism, as a Model for HIV Infection.
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- ChemMedChem, 2019, v. 14, n. 4, p. 454, doi. 10.1002/cmdc.201800718
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Evaluation of Substituted 1,2,3-Dithiazoles as Inhibitors of the Feline Immunodeficiency Virus (FIV) Nucleocapsid Protein via a Proposed Zinc Ejection Mechanism.
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- ChemMedChem, 2016, v. 11, n. 19, p. 2119, doi. 10.1002/cmdc.201600260
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Bonding features in Appel's salt from the orbital‐free quantum crystallographic perspective.
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- Acta Crystallographica Section B: Structural Science, Crystal Engineering & Materials, 2021, v. 77, n. 4, p. 478, doi. 10.1107/S2052520621005928
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Methyl 6,7-Difluoro-2-[(4-fluorobenzyl)sulfanyl]-4-hydroxyquinoline-3-carboxylate.
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- Molbank, 2024, v. 2024, n. 4, p. M1889, doi. 10.3390/M1889
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1-(Dicyanomethylene)-3-hydroxy-1 H -indene-2-carboxylic Acid.
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- Molbank, 2024, v. 2024, n. 3, p. M1871, doi. 10.3390/M1871
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5-(9-(p -Tolyl)-2,3,4,4a,9,9a-hexahydro-1 H -1,4-methanocarbazol-6-yl)thiophene-2-carbaldehyde.
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- Molbank, 2024, v. 2024, n. 1, p. M1792, doi. 10.3390/M1792
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4-(2,5-Dimethyl-1 H -pyrrol-1-yl)-1,2,5-oxadiazol-3-amine.
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- Molbank, 2023, v. 2023, n. 3, p. M1700, doi. 10.3390/M1700
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- Article
Benzo[1,2- d :4,5- d ′]bis([1,2,3]thiadiazole)-4-carbonitrile.
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- Molbank, 2023, v. 2023, n. 3, p. M1683, doi. 10.3390/M1683
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5,6-Dihydro-[1,2,5]oxadiazolo[3,4- d ]pyridazine-4,7-dione.
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- Molbank, 2023, v. 2023, n. 2, p. M1649, doi. 10.3390/M1649
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tert -Butyl (E)-3-oxo-2-(3-oxoisobenzofuran-1(3 H)-ylidene)butanoate.
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- Molbank, 2023, v. 2023, n. 2, p. M1614, doi. 10.3390/M1614
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4,4′-Difluoro-[3,3′-bi(1,2,5-oxadiazole)] 2,2′-Dioxide.
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- Molbank, 2023, v. 2023, n. 1, p. M1596, doi. 10.3390/M1596
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2-((4-(2-Ethylhexyl)-1,2,3,3 a ,4,8 b -hexahydrocyclopenta[ b ]indol-7-yl)methylene)malononitrile.
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- Molbank, 2022, v. 2022, n. 4, p. M1490, doi. 10.3390/M1490
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4,4-Bis(2-ethylhexyl)-6-(9-(2-ethylhexyl)-2,3,4,4a,9,9a-hexahydro-1 H -carbazol-6-yl)-4 H -cyclopenta[2,1- b :3,4- b ′]dithiophene-2-carbaldehyde.
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- Molbank, 2022, v. 2022, n. 4, p. M1486, doi. 10.3390/M1486
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4,4′-([1,2,5]Thiadiazolo[3,4- d ]pyridazine-4,7-diyl)bis(N , N -bis(4-methoxyphenyl)aniline).
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- Molbank, 2022, v. 2022, n. 4, p. M1479, doi. 10.3390/M1479
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4,7-Bis(2,3,3a,8b-tetrahydrocyclopenta[ b ]indol-4(1 H)-yl)-[1,2,5]thiadiazolo[3,4- c ]pyridine.
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- Molbank, 2022, v. 2022, n. 3, p. M1441, doi. 10.3390/M1441
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4,7-Di(9 H -carbazol-9-yl)-[1,2,5]oxadiazolo[3,4- d ]pyridazine.
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- Molbank, 2022, v. 2022, n. 3, p. M1428, doi. 10.3390/M1428
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5,5′-(Piperazine-1,4-diyl)bis(4-chloro-3 H -1,2-dithiol-3-one).
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- Molbank, 2022, v. 2022, n. 3, p. M1411, doi. 10.3390/M1411
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N -[3-(Chloromethyl)-1,2-benzisoxazol-5-yl]acetamide.
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- Molbank, 2022, v. 2022, n. 2, p. M1389, doi. 10.3390/M1389
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3,4-Diaminopyridine-2,5-dicarbonitrile.
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- Molbank, 2022, v. 2022, n. 2, p. M1386, doi. 10.3390/M1386
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(E)-7-(4-(Diphenylamino)styryl)benzo[ c ][1,2,5]thiadiazole-4-carbonitrile.
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- Molbank, 2022, v. 2022, n. 2, p. M1385, doi. 10.3390/M1385
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5,5′-Thiobis(4-chloro-3 H -1,2-dithiole-3-thione).
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- Molbank, 2022, v. 2022, n. 2, p. M1371, doi. 10.3390/M1371
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(E)-4-(2-(7-Bromo-[1,2,5]thiadiazolo[3,4- c ]pyridin-4-yl)vinyl)- N , N -diphenylaniline.
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- Molbank, 2022, v. 2022, n. 2, p. M1368, doi. 10.3390/M1368
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4-Bromobenzo[1,2- d :4,5- d ′]bis([1,2,3]thiadiazole).
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- Molbank, 2022, v. 2022, n. 2, p. M1362, doi. 10.3390/M1362
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- Article