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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).
- Published in:
- Chemistry of Heterocyclic Compounds, 2024, v. 60, n. 7/8, p. 403, doi. 10.1007/s10593-024-03352-w
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- Article
[1,2,5]Selenadiazolo[3,4- b]pyrazines: Synthesis from 3,4-Diamino-1,2,5-selenadiazole and Generation of Persistent Radical Anions.
- Published in:
- European Journal of Organic Chemistry, 2015, v. 2015, n. 25, p. 5585, doi. 10.1002/ejoc.201500742
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- Article
Synthesis of [1,3,2]dithiazolo[4,5-b][1,2,5]oxadiazolo[3,4-e]pyrazines.
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- ARKIVOC: Online Journal of Organic Chemistry, 2011, p. 69
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- Article
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.
- Published in:
- Molecules, 2020, v. 25, n. 17, p. 3768, doi. 10.3390/molecules25173768
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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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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- Article
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.
- Published in:
- ChemMedChem, 2019, v. 14, n. 4, p. 454, doi. 10.1002/cmdc.201800718
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- Article
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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- Article
Ethyl 11a,12-Dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine-5a(6H)-carboxylate.
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- Molbank, 2020, v. 2020, n. 3, p. M1149, doi. 10.3390/M1149
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- Article
Fused 1,2,3-Thiaselenazoles Synthesized from 1,2,3-Dithiazoles through Selective Chalcogen Exchange.
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- Chemistry - A European Journal, 2017, v. 23, n. 67, p. 17037, doi. 10.1002/chem.201703182
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- Article
New Charge-Transfer Complexes with 1,2,5-Thiadiazoles as Both Electron Acceptors and Donors Featuring an Unprecedented Addition Reaction.
- Published in:
- Chemistry - A European Journal, 2017, v. 23, n. 4, p. 852, doi. 10.1002/chem.201604121
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- Article