Perspective in Green Chemistry for Organoselenium Compounds (no more an oxymoron)

Author(s): Claudio Santi*.

Journal Name: Current Green Chemistry

Volume 6 , Issue 1 , 2019

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[1]
Santi, C.; Tidei, C.; Scalera, C.; Piroddi, M.; Galli, F. Selenium containing compounds from poison to drug candidates: A review on the GPx-like activity. Curr. Chem. Biol., 2013, 7, 25-36.
[2]
Lenardão, E.J.; Santi, C.; Sancineto, L. Bioactive organoselenium compounds and therapeutic perspectives. In: New frontiers in organoselenium compounds. Springer 2018, 99-143.
[3]
Freudendahl, D.M.; Santoro, S.; Shahzad, S.A.; Santi, C.; Wirth, T. Green chemistry with selenium reagents: Development of efficient catalytic reac- tions. Angew. Chem. Int. Ed., 2009, 48, 8409-8411.
[4]
Santoro, S.; Azeredo, J.B.; Nascimento, V.; Sancineto, L.; Braga, A.L.; Santi, C. The green side of the moon: Ecofriendly aspects of organoselenium chemistry. RSC Adv., 2014, 4, 31521-31535.
[5]
Juliano, B.A.; Ricardo, S.S.; Antonio, L.B. Synthesis of biologically active selenium-containing molecules from greener perspectives. Curr. Green Chem., 2016, 3, 51-67.
[6]
Movassagh, B.; Mohammadi, E. Green trends in synthesis of alkenyl and alkynyl chalcogenides. Curr. Green Chem., 2016, 3, 18-35.
[7]
Monti, B.; Santi, C.; Bagnoli, L.; Marini, F.; Sancineto, L. Zinc chalcogenolates as green reagents. Curr. Green Chem., 2016, 3, 68-75.
[8]
Agata, J.P.; Jacek, Ś. Terpenes as green starting materials for new organoselenium and organotellurium compounds. Curr. Green Chem., 2016, 3, 36-50.
[9]
Thomas, G.B. Oxidations catalyzed by seleninic acids and anhydrides, their precursors and congeners. Curr. Green Chem., 2016, 3, 76-91.
[10]
Santoro, S.; Santi, C.; Sabatini, M.; Testaferri, L.; Tiecco, M. Eco-friendly olefin dihydroxylation catalyzed by diphenyl diselenide. Adv. Synth. Catal., 2008, 350, 2881-2884.
[11]
Santi, C.; Di Lorenzo, R.; Tidei, C.; Bagnoli, L.; Wirth, T. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes. Tetrahedron, 2012, 68, 10530-10535.
[12]
Sancineto, L.; Mangiavacchi, F.; Tidei, C.; Bagnoli, L.; Marini, F.; Gioiello, A.; Scianowski, J.; Santi, C. Selenium-catalyzed oxacyclization of alkenoic acids and alkenols. Asian J. Org. Chem., 2017, 6, 988-992.
[13]
Sancineto, L.; Tidei, C.; Bagnoli, L.; Marini, F.; Lenardão, E.; Santi, C. Selenium catalyzed oxidation of aldehydes: Green synthesis of carboxylic acids and esters. Molecules, 2015, 20, 10496-10510.
[14]
Cerra, B.; Mangiavacchi, F.; Santi, C.; Lozza, A.M.; Gioiello, A. Selective continuous flow synthesis of hydroxy lactones from alkenoic acids. React. Chem. Eng., 2017, 2, 467-471.
[15]
Sancineto, L.; Pinto Vargas, J.; Monti, B.; Arca, M.; Lippolis, V.; Perin, G.; Lenardao, E.; Santi, C. Atom efficient preparation of zinc selenates for the synthesis of selenol esters under “on water” conditions. Molecules, 2017, 22(6), 953.
[16]
Santi, C.; Jacob, R.; Monti, B.; Bagnoli, L.; Sancineto, L.; Lenardão, E. Water and aqueous mixtures as convenient alternative media for organoselenium chemistry. Molecules, 2016, 21, 1482.
[17]
Perin, G.; Alves, D.; Jacob, R.G.; Barcellos, A.B.; Soares, L.K.; Lenardao, E.J. Synthesis of organochalcogen compounds using non‐conventional reaction media. Chem. Select., 2016, 1, 205-258.
[18]
Penteado, F.; Monti, B.; Sancineto, L.; Perin, G.; Jacob, R.G.; Santi, C.; Lenardão, E.J. Ultrasound-assisted multicomponent reactions, organometallic and organochalcogen chemistry. Asian J. Org. Chem., 2018, 7, 2368-2385.


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Article Details

VOLUME: 6
ISSUE: 1
Year: 2019
Page: [9 - 11]
Pages: 3
DOI: 10.2174/221334610601190329164654

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