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Author(s): Damiano Tanini

Journal Name: Current Chemical Biology

Volume 15 , Issue 2 , 2021


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[1]
Capperucci A, Coronnello M, Salvini F, et al. Synthesis of functionalised organochalcogenides and in vitro evaluation of their antioxidant activity. Bioorg Chem 2021; 110104812
[http://dx.doi.org/doi.org/10.1016/j.bioorg.2021.104812]
[2]
Tanini D, Trapani F, Capperucci A. 1,3,5-Trithianes and sulfur monochloride/sodium sulfide: an alternative route to 3,5-disubstituted 1,2,4-trithiolanes. J Sulfur Chem 2020; 41: 635-44.
[http://dx.doi.org/doi.org/10.1080/17415993.2020.1810251]
[3]
Tanini D, Capperucci A, Supuran CT, Angeli A. Sulfur, selenium and tellurium containing amines act as effective carbonic anhydrase activators. Bioorg Chem 2019; 87: 516-22.
[http://dx.doi.org/doi.org/10.1016/j.bioorg.2019.03.062]
[4]
Tanini D, Capperucci A, Ferraroni M, Carta F, Angeli A, Supuran CT. Direct and straightforward access to substituted alkyl selenols as novel carbonic anhydrase inhibitors. Eur J Med Chem 2020; 185111811
[http://dx.doi.org/doi.org/10.1016/j.ejmech.2019.111811]
[5]
Tanini D, D’Esopo V, Tatini D, Ambrosi M, Lo Nostro P, Capperucci A. Selenated and sulfurated analogues of triacyl glycerols: selective synthesis and structural characterization. Chemistry 2020; 26(12): 2719-25.
[http://dx.doi.org/doi.org/10.1002/chem.201904686]
[6]
Tanini D, Ricci L, Capperucci A, et al. Synthesis of novel tellurides bearing benzensulfonamide moiety as carbonic anhydrase inhibitors with antitumor activity. Eur J Med Chem 2019; 181111586
[http://dx.doi.org/doi.org/10.1016/j.ejmech.2019.111586]
[7]
Angeli A, Carta F, Donnini S, et al. Selenolesterase enzyme activity of carbonic anhydrases. Chem Commun (Camb) 2020; 56(32): 4444-7.
[http://dx.doi.org/doi.org/10.1039/d0cc00995d ]
[8]
Tanini D, Ricci L, Capperucci A. Rongalite-Promoted on water synthesis of functionalised tellurides and ditellurides. Adv Synth Catal 2020; 362: 1323-32.
[http://dx.doi.org/doi.org/10.1002/adsc.201901536 ]
[9]
Viglianisi C, Vasa K, Tanini D, et al. Ditocopheryl sulfides and disulfides: Synthesis and antioxidant profile. Chemistry 2019; 25(38): 9108-16.
[http://dx.doi.org/doi.org/10.1002/chem.201901537 ]
[10]
Tanini D, Lupori B, Malevolti G, Ambrosi M, Nostro PL, 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): 5705-8.
[http://dx.doi.org/doi.org/10.1039/c9cc02427a]


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Article Details

VOLUME: 15
ISSUE: 2
Year: 2021
Published on: 15 September, 2021
Page: [127 - 127]
Pages: 1
DOI: 10.2174/221279681502210809152428

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