Catalyst- and metal-free C(sp2)–H bond selenylation of (N-hetero)-arenes using diselenides and trichloroisocyanuric acid at room temperature

[1]  A. Lei,et al.  Electrochemical Mn-Promoted Radical Selenylation of Boronic Acids with Diselenide Reagents. , 2022, Organic letters.

[2]  A. Zamoner,et al.  IP-Se-06, a Selenylated Imidazo[1,2-a]pyridine, Modulates Intracellular Redox State and Causes Akt/mTOR/HIF-1α and MAPK Signaling Inhibition, Promoting Antiproliferative Effect and Apoptosis in Glioblastoma Cells , 2022, Oxidative medicine and cellular longevity.

[3]  D. Back,et al.  Palladium-Catalyzed Cascade 5-endo-dig Cyclization of Ynamides to Form 4-Alkynyloxazolones. , 2022, The Journal of organic chemistry.

[4]  Lokman H. Choudhury,et al.  Visible Light-Mediated C(sp2)-H Selenylation of Amino Pyrazole and Amino Uracils in the Presence of Rose Bengal as an Organophotocatalyst. , 2022, The Journal of organic chemistry.

[5]  Yun-Bing Zhou,et al.  Synthesis of Organoselenium Compounds with Elemental Selenium , 2021, Advanced Synthesis & Catalysis.

[6]  Wenjie Liu,et al.  N‐Iodosuccinimide‐promoted regioselective selenylation of 4H‐pyrido‐[1,2‐a]‐pyrimidin‐4‐ones with diselenides at room temperature , 2021, Asian Journal of Organic Chemistry.

[7]  M. Koketsu,et al.  Diorganyl diselenides: a powerful tool for the construction of selenium containing scaffolds. , 2021, Dalton transactions.

[8]  A. Arora,et al.  Preformed molecular complexes of metals with organoselenium ligands: Syntheses and applications in catalysis , 2021, Coordination Chemistry Reviews.

[9]  A. L. Braga,et al.  KIO4-mediated selective hydroxymethylation /methylenation of imidazo-heteroarenes: a greener approach. , 2021, Angewandte Chemie.

[10]  Xinquan Hu,et al.  Trichloroisocyanuric Acid‐Promoted Synthesis of Arylselenides and Aryltellurides from Diorganyl Dichalcogenides and Arylboronic Acids at Ambient Temperature , 2021 .

[11]  A. D. de Bem,et al.  A selanylimidazopyridine (3-SePh-IP) reverses the prodepressant- and anxiogenic-like effects of a high-fat/high-fructose diet in mice. , 2021, The Journal of pharmacy and pharmacology.

[12]  P. Schneider,et al.  Light‐Mediated Seleno‐Functionalization of Organic Molecules: Recent Advances , 2021, Chemical record.

[13]  D. Kundu Synthetic strategies for aryl/heterocyclic selenides and tellurides under transition-metal-catalyst free conditions , 2021, RSC advances.

[14]  E. Lenardão,et al.  Greening the synthesis of selenium-containing heterocycles: Recent efforts and advances , 2020 .

[15]  A. Zamoner,et al.  Apoptosis oxidative damage‐mediated and antiproliferative effect of selenylated imidazo[1,2‐a]pyridines on hepatocellular carcinoma HepG2 cells and in vivo , 2020, Journal of biochemical and molecular toxicology.

[16]  Qi-long Li,et al.  Organoselenium chemistry-based polymer synthesis , 2020 .

[17]  J. F. Felix,et al.  Borophosphate glass as an active media for CuO nanoparticle growth: an efficient catalyst for selenylation of oxadiazoles and application in redox reactions , 2020, Scientific Reports.

[18]  Renata A. Balaguez,et al.  Trihaloisocyanuric acids in ethanol: an eco-friendly system for the regioselective halogenation of imidazo-heteroarenes , 2020 .

[19]  I. H. Bechtold,et al.  Selenylated-oxadiazoles as promising DNA intercalators: Synthesis, electronic structure, DNA interaction and cleavage , 2020, Dyes and Pigments.

[20]  F. Dal-Pizzol,et al.  Synthesis of Novel Selenocyanates and Evaluation of Their Effect in Cultured Mouse Neurons Submitted to Oxidative Stress , 2020, Oxidative medicine and cellular longevity.

[21]  P. Evans,et al.  A Simple Zinc-Mediated Method for Selenium Addition to Michael Acceptors , 2020, Molecules.

[22]  Hualiang Jiang,et al.  Structure of Mpro from SARS-CoV-2 and discovery of its inhibitors , 2020, Nature.

[23]  Jamal Rafique,et al.  Frontispiece: Photoinduced, Direct C(sp 2 )−H Bond Azo Coupling of Imidazoheteroarenes and Imidazoanilines with Aryl Diazonium Salts Catalyzed by Eosin Y , 2020, Chemistry – A European Journal.

[24]  Ricardo F. Affeldt,et al.  Eosin Y-catalyzed photo-induced direct C(sp2)-H bond azo coupling of imidazo-heteroarenes and anilines with aryl diazonium salts. , 2019, Chemistry.

[25]  Tianfeng Chen,et al.  Rational design and action mechanisms of chemically innovative organoselenium in cancer therapy. , 2019, Chemical communications.

[26]  A. Hajra,et al.  Iodine-Catalyzed Selenylation of 2H-Indazole. , 2019, The Journal of organic chemistry.

[27]  Mi Yan,et al.  Indole: A privileged scaffold for the design of anti-cancer agents. , 2019, European journal of medicinal chemistry.

[28]  M. V. Silveira,et al.  Rice straw ash extract, an efficient solvent for regioselective hydrothiolation of alkynes , 2019, Environmental Chemistry Letters.

[29]  A. Capperucci,et al.  Ring opening reactions of heterocycles with selenium and tellurium nucleophiles , 2019, New Journal of Chemistry.

[30]  A. Porcheddu,et al.  Trichloroisocyanuric Acid: a Versatile and Efficient Chlorinating and Oxidizing Reagent , 2019, European Journal of Organic Chemistry.

[31]  A. Koner,et al.  An efficient copper-catalyzed synthesis of symmetrical bis(N-arylbenzamide) selenides and their conversion to hypervalent spirodiazaselenuranes and hydroxy congeners. , 2019, Dalton transactions.

[32]  V. Rathore,et al.  Visible-light-induced metal and reagent-free oxidative coupling of sp2 C–H bonds with organo-dichalcogenides: synthesis of 3-organochalcogenyl indoles , 2019, Green Chemistry.

[33]  L. Savegnago,et al.  Effects of a selanylimidazopyridine on the acute restraint stress-induced depressive- and anxiety-like behaviors and biological changes in mice , 2019, Behavioural Brain Research.

[34]  Peng Yang,et al.  An indole-based aerogel for enhanced removal of heavy metals from water via the synergistic effects of complexation and cation–π interactions , 2019, Journal of Materials Chemistry A.

[35]  B. Ranu,et al.  Transition Metal- and Oxidant-Free Base-Mediated Selenation of Bicyclic Arenes at Room Temperature , 2018, ACS omega.

[36]  A. L. Braga,et al.  Copper‐Catalyzed Three‐Component Reaction of Oxadiazoles, Elemental Se/S and Aryl Iodides: Synthesis of Chalcogenyl (Se/S)‐Oxadiazoles , 2018, ChemistrySelect.

[37]  A. L. Braga,et al.  KIO3 -Catalyzed C(sp2 )-H Bond Selenylation/Sulfenylation of (Hetero)arenes: Synthesis of Chalcogenated (Hetero)arenes and their Evaluation for Anti-Alzheimer Activity , 2018, Asian Journal of Organic Chemistry.

[38]  D. Back,et al.  Electrophilic Cyclization Involving Carbon-Selenium/Carbon-Halide Bond Formation: Synthesis of 3-Substituted Selenophenes. , 2018, The Journal of organic chemistry.

[39]  Shengjie Li,et al.  Recent Advances , 2018, Journal of Optimization Theory and Applications.

[40]  L. Ackermann,et al.  C4–H indole functionalisation: precedent and prospects , 2018, Chemical science.

[41]  A. L. Braga,et al.  Direct, Metal-free C(sp2 )-H Chalcogenation of Indoles and Imidazopyridines with Dichalcogenides Catalysed by KIO3. , 2018, Chemistry.

[42]  Haipu Li,et al.  Occurrence and factors affecting the formation of trihalomethanes, haloacetonitriles and halonitromethanes in outdoor swimming pools treated with trichloroisocyanuric acid , 2018 .

[43]  Li‐Zhu Wu,et al.  Visible-light-mediated aerobic selenation of (hetero)arenes with diselenides , 2017 .

[44]  Yahong Li,et al.  New fluorescent imidazo[1,2-a]pyridine-BODIPY chromophores: Experimental and theoretical approaches, and cell imaging exploration , 2017 .

[45]  Rohit K. Sharma,et al.  Insights into selenylation of imidazo[1,2-a]pyridine: synthesis, structural and antimicrobial evaluation , 2017 .

[46]  A. L. Braga,et al.  DMSO/iodine-catalyzed oxidative C–Se/C–S bond formation: a regioselective synthesis of unsymmetrical chalcogenides with nitrogen- or oxygen-containing arenes , 2016 .

[47]  R. Hondal,et al.  Why Nature Chose Selenium. , 2016, ACS chemical biology.

[48]  R. F. Canto,et al.  Recent Advances in the Synthesis of Biologically Relevant Selenium-containing 5-Membered Heterocycles , 2015 .

[49]  S. Santra,et al.  Synthesis of Imidazo[1,2‐a]pyridines: A Decade Update , 2015 .

[50]  Kai Bao,et al.  3-(3,4,5-Trimethoxyphenylselenyl)-1H-indoles and their selenoxides as combretastatin A-4 analogs: microwave-assisted synthesis and biological evaluation. , 2015, European journal of medicinal chemistry.

[51]  A. L. Braga,et al.  Solvent‐Free Fmoc Protection of Amines Under Microwave Irradiation , 2013 .

[52]  H. Sies,et al.  Chemistry of biologically important synthetic organoselenium compounds. , 2001, Chemical reviews.

[53]  C. Andersson,et al.  Synthesis, antioxidant properties, biological activity and molecular modelling of a series of chalcogen analogues of the 5-lipoxygenase inhibitor DuP 654. , 1995, Bioorganic & medicinal chemistry.

[54]  I. C. Bellettini,et al.  Synthesis of silver nanoparticles coupled with aromatic diselenides: greener approach, potential against glioma cells and DNA interaction , 2023, New Journal of Chemistry.

[55]  E. Junca,et al.  Selenylated indoles: synthesis, effects on lipid membranes properties and DNA Cleavage , 2023, New Journal of Chemistry.