Lowig, C.J. Poggendorff’s. Ann. Phys., 1836, 37, 552.

(a) Huguet, J.L. Oxidation of olefins catalyzed by selenium. Adv. Chem. Ser., 1967, 76, 345-351.
[http://dx.doi.org/10.1021/ba-1968-0076.ch051];
(b) Jones, D.N.; Mundy, D.; Whitehouse, R.D. Steroidal selenoxides diastereoisomeric at selenium; syn-elimination, absolute configuration, and optical rotatory dispersion characteristics. J. Chem. Soc. D, 1970, 86-87(2), 86.
[http://dx.doi.org/10.1039/c29700000086];
(c) Walter, R.; Roy, J. Selenomethionine, a potential catalytic antioxidant in biological systems. J. Org. Chem., 1971, 36(17), 2561-2563.
[http://dx.doi.org/10.1021/jo00816a045] [PMID: 5133874]

(a) Wilkins, L.C.; Günther, B.A.R.; Walther, M.; Lawson, J.R.; Wirth, T.; Melen, R.L. Contrasting frustrated lewis pair reactivity with selenium- and boron-based lewis acids. Angew. Chem. Int. Ed. Engl., 2016, 55(37), 11292-11295.
[http://dx.doi.org/10.1002/anie.201605239] [PMID: 27484052];
(b) Tancock, J.; Wirth, T. Selenium-mediated synthesis of tetrasubstituted naphthalenes through rearrangement. Molecules, 2015, 20(6), 10866-10872.
[http://dx.doi.org/10.3390/molecules200610866] [PMID: 26076108];
(c) Shahzad, S.A.; Vivant, C.; Wirth, T. Selenium-mediated synthesis of biaryls through rearrangement. Org. Lett., 2010, 12(6), 1364-1367.
[http://dx.doi.org/10.1021/ol100274e] [PMID: 20178316];
(d) Shahzad, S.A.; Wirth, T. Fast synthesis of benzofluorenes by selenium-mediated carbocyclizations. Angew. Chem. Int. Ed. Engl., 2009, 48(14), 2588-2591.
[http://dx.doi.org/10.1002/anie.200806148] [PMID: 19241429];
(e) Freudendahl, D.M.; Shahzad, S.A.; Wirth, T. Recent advances in organoselenium chemistry. Eur. J. Org. Chem., 2009, 2009(11), 1649-1664.
[http://dx.doi.org/10.1002/ejoc.200801171];
(f) Freudendahl, D.M.; Santoro, S.; Shahzad, S.A.; Santi, C.; Wirth, T. Green chemistry with selenium reagents: Development of efficient catalytic reactions. Angew. Chem. Int. Ed. Engl., 2009, 48(45), 8409-8411.
[http://dx.doi.org/10.1002/anie.200903893] [PMID: 19802863];
(g) Browne, D. M.; Wirth, T. New developments with chiral electrophilic selenium reagents. Curr. Org. Chem., 2006, 10, 1893-1903.
[http://dx.doi.org/10.2174/138527206778521213]

(a) Santi, C.; Di Lorenzo, R.; Tidei, C.; Bagnoli, L.; Wirth, T. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes. Tetrahedron, 2012, 68(51), 10530-10535.
[http://dx.doi.org/10.1016/j.tet.2012.08.078];
(b) Singh, F.V.; Wirth, T. Selenium-catalyzed regioselective cyclization of unsaturated carboxylic acids using hypervalent iodine oxidants. Org. Lett., 2011, 13(24), 6504-6507.
[http://dx.doi.org/10.1021/ol202800k] [PMID: 22085140];
(c) Singh, F.V.; Wirth, T. Organoselenium Chemistry; Wirth, T., Ed.; Wiley-VCH, 2011, pp. 321-356.
[http://dx.doi.org/10.1002/9783527641949.ch8];
(d) Browne, D.M.; Niyomura, O.; Wirth, T. Catalytic use of selenium electrophiles in cyclizations. Org. Lett., 2007, 9(16), 3169-3171.
[http://dx.doi.org/10.1021/ol071223y] [PMID: 17608489];
(e) Braga, A.L.; Ludtke, D.S.; Vargas, F.; Braga, R.C. Catalytic applications of chiral organoselenium compounds in asymmetric synthesis. Synlett, 2006, 10(10), 1453-1466.
[http://dx.doi.org/10.1055/s-2006-941592]

(a) Thomas, S.P.; Satheeshkumar, K.; Mugesh, G.; Guru Row, T.N. Unusually short chalcogen bonds involving organoselenium: Insights into the Se-N bond cleavage mechanism of the antioxidant ebselen and analogues. Chemistry, 2015, 21(18), 6793-6800.
[http://dx.doi.org/10.1002/chem.201405998] [PMID: 25766307];
(b) Wirth, T. Small organoselenium compounds: More than just glutathione peroxidase mimics. Angew. Chem. Int. Ed. Engl., 2015, 54(35), 10074-10076.
[http://dx.doi.org/10.1002/anie.201505056] [PMID: 26192066];
(c) Akhoon, S.A.; Naqvi, T.; Nisar, S.; Rizvi, M.A. Synthestic organo- selenium compounds in medicinal domain. Asian J. Chem., 2015, 27(8), 2745-2752.
[http://dx.doi.org/10.14233/ajchem.2015.18834];
(d) Singh, V.P.; Poon, J-F.; Butcher, R.J.; Engman, L. Pyridoxine-derived organoselenium compounds with glutathione peroxidase-like and chain-breaking antioxidant activity. Chemistry, 2014, 20(39), 12563-12571.
[http://dx.doi.org/10.1002/chem.201403229] [PMID: 25123932];
(e) Nascimento, V.; Alberto, E.E.; Tondo, D.W.; Dambrowski, D.; Detty, M.R.; Nome, F.; Braga, A.L. GPx-Like activity of selenides and selenoxides: Experimental evidence for the involvement of hydroxy perhydroxy selenane as the active species. J. Am. Chem. Soc., 2012, 134(1), 138-141.
[http://dx.doi.org/10.1021/ja209570y] [PMID: 22136421]

(a) Flohe, L.; Gunzler, E. A.; Schock, H. H. Glutathione peroxidase: A selenoenzyme. FEBS Lett., 1973, 32, 132-134.
[http://dx.doi.org/10.1016/0014-5793(73)80755-0];
(b) Rotruck, J.T.; Pope, A.L.; Ganther, H.E.; Swanson, A.B.; Hafeman, D.G.; Hoekstra, W.G. Selenium: Biochemical role as a component of glutathione peroxidase. Science, 1973, 179, 588-590.
[http://dx.doi.org/10.1126/science.179.4073.588]

(a) Behne, D.; Kyriakopoulos, A.; Meinhold, H.; Köhrle, J. Identification of type I iodothyronine 5′-deiodinase as a selenoenzyme. Biochem. Biophys. Res. Commun., 1990, 173(3), 1143-1149.
[http://dx.doi.org/10.1016/S0006-291X(05)80905-2] [PMID: 2268318];
(b) Köhrle, J. Iodothyronine deiodinases. Methods Enzymol., 2002, 347, 125-167.
[http://dx.doi.org/10.1016/S0076-6879(02)47014-0] [PMID: 11898402]

Tamura, T.; Stadtman, T.C. A new selenoprotein from human lung adenocarcinoma cells: Purification, properties, and thioredoxin reductase activity. Proc. Natl. Acad. Sci. USA, 1996, 93(3), 1006-1011.
[http://dx.doi.org/10.1073/pnas.93.3.1006] [PMID: 8577704]

(a) Wirth, T. Organoselenium Chemistry: Synthesis and Reactions; Wiley-VCH: Germany, 2011.
[http://dx.doi.org/10.1002/9783527641949];
(b) Patai, S.; Rappoport, Z. The Chemistry of Organic Selenium and Tellurium Compounds; John Wiley, 2012, p. 3.;
(c) Back, T.G. Organoselenium Chemistry; Oxford University Press: Oxford, 1999. ;
(d) Wirth, T. Organoselenium chemistry: Modern developments in organic synthesis. Top. Curr. Chem., 2000, 208, 259.
[http://dx.doi.org/10.1007/3-540-48171-0_1];
(e) Liotta, D. Organoselenium Chemistry; John Wiley & Sons: New York, 1987. ;
(f) Paulmier, C. Selenium Reagents and Intermediates in Organic Synthesis; Pergamon Press: Oxford, 1986. ;
(g) Patai, S.; Rappoport, Z. The Chemistry of Organic Selenium and Tellurium Compounds; Wiley, 1986, p. 1.
[http://dx.doi.org/10.1002/9780470771761];
(h) Patai, S.; Rappoport, Z. The Chemistry of Organic Selenium and Tellurium Compounds; Wiley, 1987, p. 2.;
(i) Nicolaou, K.C.; Petasis, N.A. Selenium in Natural Products Synthesis; CIS: Philadelphia, 1984. ;
(j) Krief, A.; Hevesi, L. Organoselenium Chemistry I; Springer: Berlin, 1988.
[http://dx.doi.org/10.1007/978-3-642-73241-6];
(k) Klayman, D.L.; Günther, W.H.H Organic Selenium Compounds: Their Chemistry and Biology; Wiley: New York, 1973.

(a) Bhuyan, B.J.; Lamani, D.S.; Mugesh, G.; Wirth, T. Handbook of Chalcogen Chemistry: New Perspectives in Sulfur, Selenium and Tellurium; Devillanova, F.A.; du Mont, W.W., Eds.; RSC, 2013, 2, pp. 25-46.;
(b) Bhowmick, D.; Mugesh, G. Patai Series: Organic Selenium and Tellurium Compounds; Rappoport, Z., Ed.; John Wiley & Sons, 2013, 4, p. 1175.;
(c) Braga, A.L.; Rafique, J. Patai Series: Organic Selenium and Tellurium Compounds; Rappoport, Z., Ed.; John Wiley & Sons, 2014, Vol. 4, p. 1175.;
(d) Singh, F.V.; Wirth, T. Patai Series: Organic Selenium and Tellurium Compounds; Rappoport, Z., Ed.; John Wiley & Sons, 2012, Vol. 3, p. 303.;
(e) Nogueira, C.W.; Rocha, J.B.T. Patai Series: Organic Selenium and Tellurium Compounds; Rappoport, Z., Ed.; John Wiley & Sons, 2012, Vol. 3, p. 1277.;
(f) Freudendahl, D.M.; Wirth, T. Selenium and Tellurium Chemistry; Woolins, J.D.; Laitinen, R.S., Eds.; Springer, 2011, p. 41.
[http://dx.doi.org/10.1007/978-3-642-20699-3_2];
(g) Bhujan, B.J.; Mugesh, G. Organoselenium Chemistry; Wirth, T., Ed.; Wiley-VCH, 2011, p. 361.;
(h) Beaulieu, P.L.; Déziel, R. Organoselenium Chemistry: A Practical Approach; Back, T.G., Ed.; Oxford University Press: Oxford, 1999, p. 35.;
(i) Nishibayashi, Y.; Uemura, S. Topics in Current Chemistry; Wirth, T., Ed.; , 2000, 208, p. 201.

(a) Reich, H.J.; Hondal, R.J. Why nature chose selenium. ACS Chem. Biol., 2016, 11(4), 821-841.
[http://dx.doi.org/10.1021/acschembio.6b00031] [PMID: 26949981];
(b) Braga, A.L.; Barbosa, F.A.R.; Saba, S.; Canto, R.F.S.; Rafique, J. Recent advances in the synthesis of biologically relevant selenium-containing 5-membered heterocycles. Curr. Org. Chem., 2016, 20, 166-188.;
(c) Ninomiya, M.; Garud, D.R.; Koketsu, M. Biologically significant selenium-containing heterocycles. Coord. Chem. Rev., 2011, 255(23-24), 2968-2990.
[http://dx.doi.org/10.1016/j.ccr.2011.07.009];
(d) Mukherjee, A.J.; Zade, S.S.; Singh, H.B.; Sunoj, R.B. Organoselenium chemistry: role of intramolecular interactions. Chem. Rev., 2010, 110(7), 4357-4416.
[http://dx.doi.org/10.1021/cr900352j] [PMID: 20384363];
(e) Alberto, E.E.; do Nascimentob, V.; Braga, A.L. Catalytic application of selenium and tellurium compounds as glutathione peroxidase enzyme mimetics. J. Braz. Chem. Soc., 2010, 21(11), 2032-2041.
[http://dx.doi.org/10.1590/S0103-50532010001100004];
(f) Bhabak, K.P.; Mugesh, G. Functional mimics of glutathione peroxidase: Bioinspired synthetic antioxidants. Acc. Chem. Res., 2010, 43(11), 1408-1419.
[http://dx.doi.org/10.1021/ar100059g] [PMID: 20690615];
(g) Sarma, B.K.; Mugesh, G. Thiol cofactors for selenoenzymes and their synthetic mimics. Org. Biomol. Chem., 2008, 6(6), 965-974.
[http://dx.doi.org/10.1039/b716239a] [PMID: 18327317];
(h) Mlochowski, J.; Kloc, K.; Lisiak, R.; Potaczek, P.; Wojtowicz, H. Developments in the chemistry of selenaheterocyclic compounds of practical importance in synthesis and medicinal biology. ChemInform, 2007, 6(11), 14-46.
[http://dx.doi.org/10.1002/chin.200711265];
(i) Narajji, C.; Karvekar, M.D.; Das, A.K. Biological importance of organoselenium compounds. Indian J. Pharm. Sci., 2007, 69(3), 344-351.
[http://dx.doi.org/10.4103/0250-474X.34541];
(j) Guillena, G.; Ramon, D.J. Enantioselective α-heterofunctionalisation of carbonyl compounds: Organocatalysis is the simplest approach. Tetrahedron Asymmetry, 2006, 17(10), 1465-1492.
[http://dx.doi.org/10.1016/j.tetasy.2006.05.020];
(k) Tiecco, M.; Testaferri, L.; Marini, F.; Bagnoli, L.; Santi, C.; Temperini, A.; Sternativo, S.; Tomassini, C. Asymmetric syntheses promoted by organoselenium reagents. Phosphorus Sulfur Silicon Relat. Elem., 2005, 180(3-4), 729-740.
[http://dx.doi.org/10.1080/10426500590907462];
(l) Mugesh, G.; du Mont, W-W.; Sies, H. Chemistry of biologically important synthetic organoselenium compounds. Chem. Rev., 2001, 101(7), 2125-2179.
[http://dx.doi.org/10.1021/cr000426w] [PMID: 11710243];
(m) Petragnani, N.; Stefani, H.A.; Valduga, C.J. Recent advances in selenocyclofunctionalization reactions. Tetrahedron, 2001, 57(8), 1411-1448.
[http://dx.doi.org/10.1016/S0040-4020(00)01033-4];
(n) Ren, X.; Yang, L.; Liu, J.; Su, D.; You, D.; Liu, C.; Zhang, K.; Luo, G.; Mu, Y.; Yan, G.; Shen, J. A novel glutathione peroxidase mimic with antioxidant activity. Arch. Biochem. Biophys., 2001, 387(2), 250-256.
[http://dx.doi.org/10.1006/abbi.2000.2238] [PMID: 11370848];
(o) Tiecco, M. Electrophilic selenium, selenocyclizations. Top. Curr. Chem., 2000, 208, 7-54.
[http://dx.doi.org/10.1007/3-540-48171-0_2];
(p) Mugesh, G.; Singh, H.B. Synthetic organoselenium compounds as antioxidants: Glutathione peroxidase activity. Chem. Soc. Rev., 2000, 29(5), 347-357.
[http://dx.doi.org/10.1039/a908114c];
(q) Wirth, T. Chiral selenium compounds in organic synthesis. Tetrahedron, 1999, 55(1), 1-28.
[http://dx.doi.org/10.1016/S0040-4020(98)00946-6];
(r) Takada, H.; Nishibayashi, Y.; Srivastava, S.K.; Ohe, K.; Uemura, S. Highly selective asymmetric intramolecular selenocyclisation. Phosphorus Sulfur Silicon Relat. Elem., 1998, 219(1), 136-138.
[http://dx.doi.org/10.1080/10426509808546012];
(s) Wessjohann, L.A.; Sinks, U. Benzeneselenenyl reagents in organic synthesis. J. Prakt. Chem., 1998, 340(3), 189-203.
[http://dx.doi.org/10.1002/prac.19983400302];
(t) Nishibayashi, Y.; Uemura, S. Heteroatom stabilized carbenium ions. Rev. Heteroatom Chem., 1996, 14, 83.;
(u) Tiecco, M.; Testaferri, L.; Tingoli, M.; Bagnoli, L.; Marini, F.; Santi, C.; Temperini, A. Production and reactivity of new organoselenium intermediates. Formation of carbon-oxygen and carbon-nitrogen bonds. Gazz. Chim. Ital., 1996, 126, 635-644.;
(v) Reich, H.J.; Wollowitz, S. Preparation of α, β-unsaturated carbonyl compounds and nitriles by selenoxide elimination. Org. React., 1993, 44, 1.
[http://dx.doi.org/10.1002/0471264180.or044.01];
(w) Reich, H.J. Functional group manipulation using organoselenium reagents. Acc. Chem. Res., 1979, 12(1), 22-30.
[http://dx.doi.org/10.1021/ar50133a004]

(a) Müller, A.; Cadenas, E.; Graf, P.; Sies, H. A novel biologically active seleno-organic compound--I. Glutathione peroxidase-like activity in vitro and antioxidant capacity of PZ 51 (Ebselen). Biochem. Pharmacol., 1984, 33(20), 3235-3239.
[http://dx.doi.org/10.1016/0006-2952(84)90083-2] [PMID: 6487370];
(b) Wendel, A.; Fausel, M.; Safayhi, H.; Tiegs, G.; Otter, R. A novel biologically active seleno-organic compound--II. Activity of PZ 51 in relation to glutathione peroxidase. Biochem. Pharmacol., 1984, 33(20), 3241-3245.
[http://dx.doi.org/10.1016/0006-2952(84)90084-4] [PMID: 6487371]

(a) Sarma, B.K.; Mugesh, G. Antioxidant activity of the anti-inflammatory compound ebselen: A reversible cyclization pathway via selenenic and seleninic acid intermediates. Chemistry, 2008, 14(34), 10603-10614.
[http://dx.doi.org/10.1002/chem.200801258] [PMID: 18932179];
(b) Bhabak, K.P.; Mugesh, G. Synthesis, characterization, and antioxidant activity of some ebselen analogues. Chemistry, 2007, 13(16), 4594-4601.
[http://dx.doi.org/10.1002/chem.200601584] [PMID: 17299817];
(c) Sarma, B.K.; Mugesh, G. Glutathione peroxidase (GPx)-like antioxidant activity of the organoselenium drug ebselen: Unexpected complications with thiol exchange reactions. J. Am. Chem. Soc., 2005, 127(32), 11477-11485.
[http://dx.doi.org/10.1021/ja052794t] [PMID: 16089478];
(d) Back, T.G.; Dyck, D.P. A novel camphor-derived selenenamide that acts as a glutathione peroxidase mimetic. J. Am. Chem. Soc., 1997, 119(9), 2079-2083.
[http://dx.doi.org/10.1021/ja963602k];
(e) Jacquemin, P.V.; Christiaens, L.E.; Renson, M.J.; Evers, M.J.; Dereu, N. Synthesis of 2H,3-4-Dihydro-1,2-benzoselenazin-3-one and derivatives: A new heterocyclic ring system. Tetrahedron Lett., 1992, 33(27), 3863-3866.
[http://dx.doi.org/10.1016/S0040-4039(00)74805-2];
(f) Wilson, S.R.; Zucker, P.A.; Huang, R.R.C.; Spector, P.A. Development of synthetic compounds with glutathione peroxidase activity. J. Am. Chem. Soc., 1989, 111(15), 5936-5939.
[http://dx.doi.org/10.1021/ja00197a065];
(g) Reich, H.J.; Jasperse, C.P. Organoselenium chemistry. Redox chemistry of selenocysteine model systems. J. Am. Chem. Soc., 1987, 109(18), 5549-5551.
[http://dx.doi.org/10.1021/ja00252a055]

(a) Tripathi, S.K.; Sharma, S.; Singh, H.B.; Butcher, R.J. 2-Phenoxyethanol derived diselenide and related compounds; synthesis of a seven-membered seleninate ester. Org. Biomol. Chem., 2011, 9(2), 581-587.
[http://dx.doi.org/10.1039/C0OB00038H] [PMID: 21049128];
(b) Hassan, W.; Pinton, S.; Rocha, J.T.; Deobald, A.M.; Braga, A.L.; Nogueira, C.W.; Latini, A.S.; Rocha, J.B.T. Hydroxyl containing seleno-imine compound exhibits improved anti-oxidant potential and does not inhibit thiol-containing enzymes. Chem. Biol. Interact., 2011, 190(1), 35-44.
[http://dx.doi.org/10.1016/j.cbi.2011.01.012] [PMID: 21256831];
(c) Bhabak, K.P.; Mugesh, G. Synthesis and structure-activity correlation studies of secondary- and tertiaryamine-based glutathione peroxidase mimics. Chemistry, 2009, 15(38), 9846-9854.
[http://dx.doi.org/10.1002/chem.200900818] [PMID: 19551790];
(d) Bhabak, K.P.; Mugesh, G. A simple and efficient strategy to enhance the antioxidant activities of amino-substituted glutathione peroxidase mimics. Chemistry, 2008, 14(28), 8640-8651.
[http://dx.doi.org/10.1002/chem.200800963] [PMID: 18668498];
(e) Mugesh, G.; Panda, A.; Singh, H.B.; Punekar, N.S.; Butcher, R.J. Glutathione peroxidase-like antioxidant activity of diaryl diselenides: A mechanistic study. J. Am. Chem. Soc., 2001, 123(5), 839-850.
[http://dx.doi.org/10.1021/ja994467p] [PMID: 11456617];
(f) Mugesh, G.; Panda, A.; Singh, H.B.; Butcher, R.J. Intramolecular Se···N nonbonding interactions in low-valent organoselenium derivatives: A detailed study by 1H and 77Se NMR spectroscopy and X-ray crystallography. Chemistry, 1999, 5(5), 1411-1421.
[http://dx.doi.org/10.1002/(SICI)1521-3765(19990503)5:5<1411::AID-CHEM1411>3.0.CO;2-M];
(g) Wirth, T. Glutathione peroxidase-like activities of oxygen-containing diselenides. Molecules, 1998, 3(8), 164-166.
[http://dx.doi.org/10.3390/30700164]

Collins, C.A.; Fry, F.H.; Holme, A.L.; Yiakouvaki, A.; Al-Qenaei, A.; Pourzand, C.; Jacob, C. Towards multifunctional antioxidants: Synthesis, electrochemistry, in vitro and cell culture evaluation of compounds with ligand/catalytic properties. Org. Biomol. Chem., 2005, 3(8), 1541-1546.
[http://dx.doi.org/10.1039/b503282m] [PMID: 15827654]

(a) Jain, V.K.; Priyadarsini, K.I. National Library of Medicine. Proc. Natl. Acad. Sci. USA, 2010, 80A, 269.;
(b) Fumakura, F.; Mishra, B.; Priyadarsini, K.I.; Iwaoka, M. A water-soluble cyclic selenide with enhanced glutathione peroxidase-like catalytic activities. Eur. J. Org. Chem., 2010, 3(3), 440-445.
[http://dx.doi.org/10.1002/ejoc.200901114];
(c) Johansson, H.; Svartström, O.; Phadnis, P.; Engman, L.; Ott, M.K. Exploring a synthetic organoselenium compound for antioxidant pharmacotherapy--toxicity and effects on ROS-production. Bioorg. Med. Chem., 2010, 18(5), 1783-1788.
[http://dx.doi.org/10.1016/j.bmc.2010.01.057] [PMID: 20156690];
(d) Plano, D.; Baquedano, Y.; Ibáñez, E.; Jiménez, I.; Palop, J.A.; Spallholz, J.E.; Sanmartín, C. Antioxidant-prooxidant properties of a new organoselenium compound library. Molecules, 2010, 15(10), 7292-7312.
[http://dx.doi.org/10.3390/molecules15107292] [PMID: 20966875];
(e) Belenky, P.; Bogan, K.L.; Brenner, C. NAD+ metabolism in health and disease. Trends Biochem. Sci., 2007, 32(1), 12-19.
[http://dx.doi.org/10.1016/j.tibs.2006.11.006] [PMID: 17161604];
(f) Back, T.G.; Moussa, Z.; Parvez, M. The exceptional glutathione peroxidase-like activity of di(3-hydroxypropyl) selenide and the unexpected role of a novel spirodioxaselenanonane intermediate in the catalytic cycle. Angew. Chem. Int. Ed., 2004, 43(10), 1268-1270.
[http://dx.doi.org/10.1002/anie.200353128] [PMID: 14991795];
(g) Rojanasakul, Y.; Ye, J.; Chen, F.; Wang, L.; Cheng, N.; Castranova, V.; Vallyathan, V.; Shi, X. Dependence of NF-kappaB activation and free radical generation on silica-induced TNF-α production in macrophages. Mol. Cell. Biochem., 1999, 200(1-2), 119-125.
[http://dx.doi.org/10.1023/A:1007051402840] [PMID: 10569191]

(a) Yu, S-C.; Borchert, A.; Kuhn, H.; Ivanov, I. Synthesis of a new seleninic acid anhydride and mechanistic studies into its glutathione peroxidase activity. Chemistry, 2008, 14(23), 7066-7071.
[http://dx.doi.org/10.1002/chem.200800694] [PMID: 18604859];
(b) Back, T.G.; Kuzma, D.; Parvez, M. Aromatic derivatives and tellurium analogues of cyclic seleninate esters and spirodioxyselenuranes that act as glutathione peroxidase mimetics. J. Org. Chem., 2005, 70(23), 9230-9236.
[http://dx.doi.org/10.1021/jo0512711] [PMID: 16268595];
(c) Zade, S.S.; Singh, H.B.; Butcher, R.J. The isolation and crystal structure of a cyclic selenenate ester derived from Bis(2,6-diformyl-4-tert-butylphenyl)diselenide and its glutathione peroxidase-like activity. Angew. Chem. Int. Ed., 2004, 43(34), 4513-4515.
[http://dx.doi.org/10.1002/anie.200460380] [PMID: 15340957];
(d) Back, T.G.; Moussa, Z. Diselenides and allyl selenides as glutathione peroxidase mimetics. Remarkable activity of cyclic seleninates produced in situ by the oxidation of allyl ω-hydroxyalkyl selenides. J. Am. Chem. Soc., 2003, 125(44), 13455-13460.
[http://dx.doi.org/10.1021/ja0357588] [PMID: 14583041];
(e) Back, T.G.; Moussa, Z. Remarkable activity of a novel cyclic seleninate ester as a glutathione peroxidase mimetic and its facile in situ generation from allyl 3-hydroxypropyl selenide. J. Am. Chem. Soc., 2002, 124(41), 12104-12105.
[http://dx.doi.org/10.1021/ja028030k] [PMID: 12371844]

Galant, L.S.; Rafique, J.; Braga, A.L.; Braga, F.C.; Saba, S.; Radi, R.; da Rocha, J.B.T.; Santi, C.; Monsalve, M.; Farina, M.; de Bem, A.F. The thiol-modifier effects of organoselenium compounds and their cytoprotective actions in neuronal cells. Neurochem. Res., 2021, 46(1), 120-130.
[http://dx.doi.org/10.1007/s11064-020-03026-x] [PMID: 32285377]

Victoria, F.N.; Anversa, R.; Penteado, F.; Castro, M.; Lenardão, E.J.; Savegnago, L. Antioxidant and antidepressant-like activities of semi-synthetic α-phenylseleno citronellal. Eur. J. Pharmacol., 2014, 742, 131-138.
[http://dx.doi.org/10.1016/j.ejphar.2014.09.005] [PMID: 25218989]

Victoria, F.N.; Radatz, C.S.; Sachini, M.; Jacob, R.G.; Perin, G.; da Silva, W.P.; Lenardao, E.J. KF/Al2O3 and PEG-400 as a recyclable medium for the selective α-selenation of aldehydes and ketones. Preparation of potential antimicrobial agents. Tetrahedron Lett., 2009, 50(49), 6761-6763.
[http://dx.doi.org/10.1016/j.tetlet.2009.09.093]

Botteselle, G.V.; Elias, W.C.; Bettanin, L.; Canto, R.F.S.; Salin, D.N.O.; Barbosa, F.A.R.; Saba, S.; Gallardo, H.; Ciancaleoni, G.; Domingos, J.B.; Rafique, J.; Braga, A.L. Catalytic antioxidant activity of bis-aniline-derived diselenides as GPx mimics. Molecules, 2021, 26(15), 4446.
[http://dx.doi.org/10.3390/molecules26154446] [PMID: 34361597]

Iwaoka, M.; Tomoda, S. A model study on the effect of an amino group on the antioxidant activity of glutathione peroxidase. J. Am. Chem. Soc., 1994, 116(6), 2557-2561.
[http://dx.doi.org/10.1021/ja00085a040]

Alberto, E.E.; Soares, L.C.; Sudati, J.H.; Borges, A.C.A.; Rocha, J.B.T.; Braga, A.L. Efficient synthesis of modular amino acid derivatives containing selenium with pronounced GPx-like activity. Eur. J. Org. Chem., 2009, 25(25), 4211-4214.
[http://dx.doi.org/10.1002/ejoc.200900485]

Sudati, J.H.; Nogara, P.A.; Saraiva, R.A.; Wagner, C.; Alberto, E.E.; Braga, A.L.; Fachinetto, R.; Piquini, P.C.; Rocha, J.B.T. Diselenoamino acid derivatives as GPx mimics and as substrates of TrxR: In vitro and in silico studies. Org. Biomol. Chem., 2018, 16(20), 3777-3787.
[http://dx.doi.org/10.1039/C8OB00451J] [PMID: 29737350]

Arai, K.; Sato, Y.; Nakajima, I.; Saito, M.; Sasaki, M.; Kanamori, A.; Iwaoka, M. Glutathione peroxidase-like functions of 1,2-diselenane-4,5-diol and its amphiphilic derivatives: Switchable catalytic cycles depending on peroxide substrates. Bioorg. Med. Chem., 2021, 29, 115866.
[http://dx.doi.org/10.1016/j.bmc.2020.115866] [PMID: 33203607]

Shaaban, S.; Vervandier-Fasseur, D.; Andreoletti, P.; Zarrouk, A.; Richard, P.; Negm, A.; Manolikakes, G.; Jacob, C.; Cherkaoui-Malki, M. Cytoprotective and antioxidant properties of organic selenides for the myelin-forming cells, oligodendrocytes. Bioorg. Chem., 2018, 80, 43-56.
[http://dx.doi.org/10.1016/j.bioorg.2018.05.019] [PMID: 29864687]

Shaaban, S.; Ashmawy, A.M.; Negm, A.; Wessjohann, L.A. Synthesis and biochemical studies of novel organic selenides with increased selectivity for hepatocellular carcinoma and breast adenocarcinoma. Eur. J. Med. Chem., 2019, 179, 515-526.
[http://dx.doi.org/10.1016/j.ejmech.2019.06.075] [PMID: 31276896]

Bhuyan, B.J.; Mugesh, G. Synthesis, characterization and antioxidant activity of angiotensin converting enzyme inhibitors. Org. Biomol. Chem., 2011, 9(5), 1356-1365.
[http://dx.doi.org/10.1039/C0OB00823K] [PMID: 21186397]

(a) Yang, H.Y.T.; Erdös, E.G.; Levin, Y. Characterization of a dipeptide hydrolase (kininase II: Angiotensin I converting enzyme). J. Pharmacol. Exp. Ther., 1971, 177(1), 291-300.
[PMID: 4327809];
(b) Erdos, E.G.; Yang, H.Y.T. An enzyme in microsomal fraction of kidney that inactivates bradykinin. Life Sci., 1967, 6(6), 569-574.
[http://dx.doi.org/10.1016/0024-3205(67)90090-2] [PMID: 4962200];
(c) Yang, H.Y.T.; Erdös, E.G. Second kininase in human blood plasma. Nature, 1967, 215(5108), 1402-1403.
[http://dx.doi.org/10.1038/2151402a0] [PMID: 6055465]

(a) Sturrock, E.D.; Natesh, R.; van Rooyen, J.M.; Acharya, K.R. Structure of angiotensin I-converting enzyme. Cell. Mol. Life Sci., 2004, 61(21), 2677-2686.
[http://dx.doi.org/10.1007/s00018-004-4239-0] [PMID: 15549168];
(b) Natesh, R.; Schwager, S.L.U.; Sturrock, E.D.; Acharya, K.R. Crystal structure of the human angiotensin-converting enzyme-lisinopril complex. Nature, 2003, 421(6922), 551-554.
[http://dx.doi.org/10.1038/nature01370] [PMID: 12540854];
(c) Ehlers, M.R.W.; Riordan, J.F. Angiotensin-converting enzyme: Zinc- and inhibitor-binding stoichiometries of the somatic and testis isozymes. Biochemistry, 1991, 30(29), 7118-7126.
[http://dx.doi.org/10.1021/bi00243a012] [PMID: 1649623];
(d) Ehlers, M.R.W.; Fox, E.A.; Strydom, D.J.; Riordan, J.F. Molecular cloning of human testicular angiotensin-converting enzyme: The testis isozyme is identical to the C-terminal half of endothelial angiotensin-converting enzyme. Proc. Natl. Acad. Sci. USA, 1989, 86(20), 7741-7745.
[http://dx.doi.org/10.1073/pnas.86.20.7741] [PMID: 2554286]

Nascimento, V.; Ferreira, N.L.; Canto, R.F.S.; Schott, K.L.; Waczuk, E.P.; Sancineto, L.; Santi, C.; Rocha, J.B.T.; Braga, A.L. Synthesis and biological evaluation of new nitrogen-containing diselenides. Eur. J. Med. Chem., 2014, 87, 131-139.
[http://dx.doi.org/10.1016/j.ejmech.2014.09.022] [PMID: 25244678]

Yang, X.; Wang, Q.; Tao, Y.; Xu, H. A modified method to prepare diselenides by the reaction of selenium with sodium borohydride. J. Chem. Res., 2002, 4(4), 160-161.
[http://dx.doi.org/10.3184/030823402103171726]

Ibrahim, M.; Hassan, W.; Anwar, J.; Deobald, A.M.; Kamdem, J.P.; Souza, D.O.; Rocha, J.B.T. 1-(2-(2-(2-(1-Aminoethyl)phenyl)diselanyl)phenyl)ethanamine: An amino organoselenium compound with interesting antioxidant profile. Toxicol., 2014, 28(4), 524-530.
[http://dx.doi.org/10.1016/j.tiv.2013.12.010] [PMID: 24394197]

(a) Braga, A.L.; Paixao, M.W.; Marin, G. Seleno-Imine: A new class of versatile, modular N, Se ligands for asymmetric palladium-catalyzed allylic alkylation. Synlett, 2005, 11(11), 1675-1678.
[http://dx.doi.org/10.1055/s-2005-871546];
(b) Liu, D.; Dai, Q.; Zhang, X. A new class of readily available and conformationally rigid phosphino-oxazoline ligands for asymmetric catalysis. Tetrahedron, 2005, 61(26), 6460-6471.
[http://dx.doi.org/10.1016/j.tet.2005.03.111]

Ibrahim, M.; Muhammad, N.; Naeem, M.; Deobald, A.M.; Kamdem, J.P.; Rocha, J.B.T. In vitro evaluation of glutathione peroxidase (GPx)-like activity and antioxidant properties of an organoselenium compound. Toxicol., 2015, 29(5), 947-952.
[http://dx.doi.org/10.1016/j.tiv.2015.03.017] [PMID: 25862122]

Hodage, A.S.; Prabhu, C.P.; Phadnis, P.P.; Wadawale, A.; Priyadarsini, K.I.; Jain, V.K. Synthesis, characterization, structures and GPx mimicking activity of pyridyl and pyrimidyl based organoselenium compounds. J. Organomet. Chem., 2012, 720, 19-25.
[http://dx.doi.org/10.1016/j.jorganchem.2012.08.035]

Bhowmick, D.; Srivastava, S.; D’Silva, P.; Mugesh, G. Highly efficient glutathione peroxidase and peroxiredoxin mimetics protect mammalian cells against oxidative damage. Angew. Chem. Int. Ed. Engl., 2015, 54(29), 8449-8453.
[http://dx.doi.org/10.1002/anie.201502430] [PMID: 26032473]

(a) Comins, D.L.; Brown, J.D. Ortho metalation directed by alpha-amino alkoxides. J. Org. Chem., 1984, 49(6), 1078-1083.
[http://dx.doi.org/10.1021/jo00180a024];
(b) Press, D.J.; McNeil, N.M.R.; Hambrook, M.; Back, T.G. Effects of methoxy substituents on the glutathione peroxidase-like activity of cyclic seleninate esters. J. Org. Chem., 2014, 79(19), 9394-9401.
[http://dx.doi.org/10.1021/jo501689h] [PMID: 25198287]

Break, L.M.; Mohamed, M.; Abdel-Hafez, S.H. Synthesis of new organoselenium compounds containing nucleosides as antioxidant. Orient. J. Chem., 2014, 30(4), 1639-1645.
[http://dx.doi.org/10.13005/ojc/300423]

Upadhyay, A.; Singh Bhakuni, B.; Meena, R.; Kumar, S. Radical chain breaking Bis(ortho-organoselenium) substituted phenolic antioxidants. Chem. Asian J., 2021, 16(8), 966-973.
[http://dx.doi.org/10.1002/asia.202100139] [PMID: 33660419]

Singh, B.G.; Kumar, P.; Phadnis, P.; Iwaoka, M.; Priyadarsini, K.I. Free radical induced selenoxide formation in isomeric organoselenium compounds: The effect of chemical structures on antioxidant activity. New J. Chem., 2019, 43(34), 13357-13362.
[http://dx.doi.org/10.1039/C9NJ02227A]

Iwaoka, M.; Takahashi, T.; Tomoda, S. Syntheses and structural characterization of water-soluble selenium reagents for the redox control of protein disulfide bonds. Heteroatom Chem., 2001, 12(4), 293-299.
[http://dx.doi.org/10.1002/hc.1047]

Bocchini, B.; Goldani, B.; Sousa, F.S.S.; Birmann, P.T.; Brüning, C.A.; Lenardão, E.J.; Santi, C.; Savegnago, L.; Alves, D. Synthesis and antioxidant activity of new selenium-containing quinolines. Med. Chem., 2021, 17(6), 667-676.
[http://dx.doi.org/10.2174/1573406416666200403081831] [PMID: 32242787]

Savegnago, L.; Vieira, A.I.; Seus, N.; Goldani, B.S.; Castro, M.R.; Lenardão, E.J.; Alves, D. Synthesis and antioxidant properties of novel quinoline–chalcogenium compounds. Tetrahedron Lett., 2013, 54(1), 40-44.
[http://dx.doi.org/10.1016/j.tetlet.2012.10.067]

Fonseca, S.F.; Lima, D.B.; Alves, D.; Jacob, R.G.; Perin, G.; Lenardao, E.J.; Savegnago, L. Synthesis, characterization and antioxidant activity of organoselenium and organotellurium compound derivatives of chrysin. New J. Chem., 2015, 39(4), 3043-3050.
[http://dx.doi.org/10.1039/C4NJ02329C]

Shaaban, S.; Zarrouk, A.; Vervandier-Fasseur, D.; Al-Faiyz, Y.S.; El-Sawy, H.; Althagafi, I.; Andreoletti, P.; Cherkaoui-Malki, M. Cytoprotective organoselenium compounds for oligodendrocytes. Arab. J. Chem., 2021, 14, 103051.
[http://dx.doi.org/10.1016/j.arabjc.2021.103051]

Sauer, A.C.; Leal, J.G.; Stefanello, S.T.; Leite, M.T.B.; Souza, M.B.; Soares, F.A.A.; Rodrigues, O.E.D.; Dornelles, L. Synthesis and antioxidant properties of organosulfur and organoselenium compounds derived from 5-substituted-1,3,4-oxadiazole/thiadiazole-2-thiols. Tetrahedron Lett., 2017, 58(1), 87-91.
[http://dx.doi.org/10.1016/j.tetlet.2016.11.106]

Bhuyan, B.J.; Mugesh, G. Antioxidant activity of peptide-based angiotensin converting enzyme inhibitors. Org. Biomol. Chem., 2012, 10(11), 2237-2247.
[http://dx.doi.org/10.1039/c2ob06533a] [PMID: 22307539]

He, X.; Nie, Y.; Zhong, M.; Li, S.; Li, X.; Guo, Y.; Liu, Z.; Gao, Y.; Ding, F.; Wen, D.; Zhang, Y. New organoselenides (NSAIDs-Se derivatives) as potential anticancer agents: Synthesis, biological evaluation and in silico calculations. Eur. J. Med. Chem., 2021, 218, 113384.
[http://dx.doi.org/10.1016/j.ejmech.2021.113384] [PMID: 33799070]

Kumar, M.; Chhillar, B.; Yadav, M.; Sagar, P.; Singhal, N.K.; Gates, P.J.; Butcher, R.J.; Singh, V.P. Catalytic and highly regenerable aminic organoselenium antioxidants with cytoprotective effects. Org. Biomol. Chem., 2021, 19(9), 2015-2022.
[http://dx.doi.org/10.1039/D0OB02368J] [PMID: 33591294]

Obieziurska-Fabisiak, M.; Pacuła, A.J.; Capoccia, L.; Drogosz-Stachowicz, J.; Janecka, A.; Santi, C.; Ścianowski, J. Phenylselanyl group incorporation for “glutathione peroxidase-like” activity modulation. Molecules, 2020, 25(15), 3354.
[http://dx.doi.org/10.3390/molecules25153354] [PMID: 32722043]

Obieziurska, M.; Pacuła, A.J.; Długosz-Pokorska, A.; Krzemiński, M.; Janecka, A.; Ścianowski, J. Bioselectivity induced by chirality of new terpenyl organoselenium compounds. Materials (Basel), 2019, 12(21), 3579.
[http://dx.doi.org/10.3390/ma12213579] [PMID: 31683558]

Obieziurska, M.; Pacuła, A.J.; Juhas, U.; Antosiewicz, J.; Ścianowski, J. The influence of O/S exchange on the biocatalytical activity of benzisoselenazol-3(2H)-ones. Catalysts, 2018, 8(11), 493.
[http://dx.doi.org/10.3390/catal8110493]

Elsherbini, M.; Hamama, W.S.; Zooroba, H.H. An easy synthetic approach to construct some ebselen analogues and Benzo[b]selenophene derivatives: Their antioxidant and cytotoxic assessment. J. Heterocycl. Chem., 2018, 55(7), 1645-1650.
[http://dx.doi.org/10.1002/jhet.3199]

Elsherbini, M.; Hamama, W.S.; Zoorob, H.H.; Bhowmick, V.; Mugesh, G.; Wirth, T. Synthesis and antioxidant activities of novel chiral ebselen analogues. Heteroatom Chem., 2014, 25(5), 320-325.
[http://dx.doi.org/10.1002/hc.21164]

Lamani, D.S.; Bhowmick, D.; Mugesh, G. Substituent effects on the stability and antioxidant activity of spirodiazaselenuranes. Molecules, 2015, 20(7), 12959-12978.
[http://dx.doi.org/10.3390/molecules200712959] [PMID: 26193249]

Sarma, B.K.; Manna, D.; Minoura, M.; Mugesh, G. Synthesis, structure, spirocyclization mechanism, and glutathione peroxidase-like antioxidant activity of stable spirodiazaselenurane and spirodiazatellurane. J. Am. Chem. Soc., 2010, 132(15), 5364-5374.
[http://dx.doi.org/10.1021/ja908080u] [PMID: 20345146]

Lamani, D.S.; Bhowmick, D.; Mugesh, G. Spirodiazaselenuranes: Synthesis, structure and antioxidant activity. Org. Biomol. Chem., 2012, 10(39), 7933-7943.
[http://dx.doi.org/10.1039/c2ob26156a] [PMID: 22932965]

McNeil, N.M.R.; Press, D.J.; Mayder, D.M.; Garnica, P.; Doyle, L.M.; Back, T.G. Enhanced glutathione peroxidase activity of water-soluble and polyethylene glycol-supported selenides, related spirodioxyselenuranes, and pincer selenuranes. J. Org. Chem., 2016, 81(17), 7884-7897.
[http://dx.doi.org/10.1021/acs.joc.6b01593] [PMID: 27525346]

Prasad, P.R.; Singh, H.B.; Butcher, R.J. Synthesis, structure and reactivity of β-chalcocyclohexenals: Dichalcogenides and chalcogenides. J. Organomet. Chem., 2016, 814, 42-56.
[http://dx.doi.org/10.1016/j.jorganchem.2016.04.019]

Gagan, J.M.F.; Lane, A.G.; Lloyd, D. The stereochemistry of β-chlorovinyl-aldehydes. J. Chem. Soc. C, 1970, 18(18), 2484-2488.
[http://dx.doi.org/10.1039/J39700002484]

Prasad, P.R.; Singh, H.B.; Butcher, R.J. Synthesis, structure and antioxidant activity of cyclohexene-fused selenuranes and related derivatives. Molecules, 2015, 20(7), 12670-12685.
[http://dx.doi.org/10.3390/molecules200712670] [PMID: 26184146]

Wang, J.; Zhao, B.; Wang, X.; Yao, J.; Zhang, J. Synthesis of selenium-containing polysaccharides and evaluation of antioxidant activity in vitro. Int. J. Biol. Macromol., 2012, 51(5), 987-991.
[http://dx.doi.org/10.1016/j.ijbiomac.2012.08.011] [PMID: 22935693]

Merino-Montiel, P.; Lopez, O.; Fernandez-Bolanos, J.G. l-Isofucoselenofagomine and derivatives: Dual activities as antioxidants and as glycosidase inhibitors. Tetrahedron, 2012, 68(18), 3591-3595.
[http://dx.doi.org/10.1016/j.tet.2012.03.003]

Ulgar, V.; Fernandez-Bolanos, J. G.; Bols, M. Synthesis and evaluation of sulfonium analogues of isofucofagomine as glycosidase inhibitors. Chem. Soc., Perkin Trans., 2002, 10, 1242-1246.
[http://dx.doi.org/10.1039/b202021c]

Merino-Montiel, P.; Maza, S.; Martos, S.; López, Ó.; Maya, I.; Fernández-Bolaños, J.G. Synthesis and antioxidant activity of O-alkyl selenocarbamates, selenoureas and selenohydantoins. Eur. J. Pharm. Sci., 2013, 48(3), 582-592.
[http://dx.doi.org/10.1016/j.ejps.2012.12.016] [PMID: 23287366]

Lopez, O.; Maza, S.; Ulgar, V.; Maya, I.; Fernandez-Bolanos, J.G. Synthesis of sugar-derived isoselenocyanates, selenoureas, and selenazoles. Tetrahedron, 2009, 65(12), 2556-2566.
[http://dx.doi.org/10.1016/j.tet.2009.01.038]

Prabhu, C.P.; Phadnis, P.P.; Wadawale, A.P.; Priyadarsini, K.I.; Jain, V.K. Synthesis, characterization, structures and antioxidant activity of nicotinoyl based organoselenium compounds. J. Organomet. Chem., 2012, 713, 42-50.
[http://dx.doi.org/10.1016/j.jorganchem.2012.04.014]

Rafique, J.; Saba, S.; Canto, R.F.S.; Frizon, T.E.A.; Hassan, W.; Waczuk, E.P.; Jan, M.; Back, D.F.; Da Rocha, J.B.T.; Braga, A.L. Synthesis and biological evaluation of 2-picolylamide-based diselenides with non-bonded interactions. Molecules, 2015, 20(6), 10095-10109.
[http://dx.doi.org/10.3390/molecules200610095] [PMID: 26039333]

Frizon, T.E.A.; Cararo, J.H.; Saba, S.; Dal-Pont, G.C.; Michels, M.; Braga, H.C.; Pimentel, T.; Dal-Pizzol, F.; Valvassori, S.S.; Rafique, J. Synthesis of novel selenocyanates and evaluation of their effect in cultured mouse neurons submitted to oxidative stress. Oxidative Med. Cell. Longev., 2020, 2020, 5417024.
[http://dx.doi.org/10.1155/2020/5417024]

Barick, K.C.; Dutta, B.; Gawali, S.L.; Phadnis, P.P.; Priyadarsini, K.I.; Jain, V.K.; Hassan, P.A. Phenylseleno N-acetyl α-amino acids conjugated magnetic nanoparticles: Synthesis, characterization and radical scavenging ability. Chem. Lett., 2020, 49(11), 1426-1430.
[http://dx.doi.org/10.1246/cl.200490]

Gao, L.; Zhuang, J.; Nie, L.; Zhang, J.; Zhang, Y.; Gu, N.; Wang, T.; Feng, J.; Yang, D.; Perrett, S.; Yan, X. Intrinsic peroxidase-like activity of ferromagnetic nanoparticles. Nat. Nanotechnol., 2007, 2(9), 577-583.
[http://dx.doi.org/10.1038/nnano.2007.260] [PMID: 18654371]

Tanini, D.; Lupori, B.; Malevolti, G.; Ambrosi, M.; Nostro, P.L.; Capperucci, A. Direct biocatalysed synthesis of first sulfur-, selenium- and tellurium- containing l-ascorbyl hybrid derivatives with radical trapping and GPx-like properties. Chem. Commun. (Camb.), 2019, 55(40), 5705-5708.
[http://dx.doi.org/10.1039/C9CC02427A] [PMID: 31033970]