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Author(s): Claudio Santi

Journal Name: Current Chemical Biology

Volume 14 , Issue 2 , 2020


DOI : 10.2174/221279681402201119090048

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[1]
Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, et al. Asymmetric azidoselenenylation of alkenes. A key step for the synthesis of enantiomerically enriched nitrogen containing compounds. Angew Chem Int Ed 2003; 42: 3131-3.
[http://dx.doi.org/10.1002/anie.200351229]
[2]
Tiecco M, Testaferri L, Santi C, Tomassini C, Bonini R, Marini F, et al. A chiral electrophilic selenium reagent to promote the kinetic resolution of racemic allylic alcohols. Org Lett 2004; 6: 4751-3.
[http://dx.doi.org/10.1002/chin.200513030]
[3]
Tiecco M, Testaferri L, Santi C, Tomassini C, Santoro S, Marini F, et al. Intramolecular nonbonding interactions between selenium and sulfur –spectroscopic evidence and importance in asymmetric synthesis. Eur J Org Chem 2006; 21: 4867-73.
[http://dx.doi.org/10.1002/ejoc.200600517]
[4]
Hayashi S, Nishide T, Nakanishi W, Sancineto L, Santi C. The nature of G⋯E–Y σ(3c–4e) in o-MenGCH2C6H4EY (MenG = Me2N and MeE; E = O, S, Se and Te; Y = F, Cl, Br, EMe and Me) with contributions from CT and compliance constants in noncovalent G⋯E interactions. RSC Advances 2019; 9(67): 39435-46.
[http://dx.doi.org/10.1039/C9RA09022C]
[5]
Freudendahl DM, Santoro S, Shahzad SA, Santi C, Wirth T. Green chemistry with selenium reagents: development of efficient catalytic reactions. Angew Chem Int Ed 2009; 48: 8409-11.
[http://dx.doi.org/10.1002/anie.200903893]
[6]
Santoro S, Azeredo JB, Nascimento V, Sancineto L, Braga AL, Santi C. The green side of the moon: Ecofriendly aspects of organoselenium chemistry. RSC Advances 2014; 4: 31521-35.
[http://dx.doi.org/10.1039/C4RA04493B]
[7]
Santoro S, Santi C, Sabatini M, Testaferri L, Tiecco M. Eco-friendly olefins dihydroxylation catalyzed by diphenyl diselenide. Adv Synth Catal 2008; 350: 2881-4.
[http://dx.doi.org/10.1002/adsc.200800571]
[8]
Mangiavacchi F, Crociani L, Sancineto L, Marini F, Santi C. Continuous bioinspired oxidation of sulfides. Molecules 2020; 25(11): 2711.
[http://dx.doi.org/10.3390/molecules25112711]
[9]
Santi C, Santoro S, Battistelli B, Testaferri L, Tiecco M. Preparation of the first bench-stable phenyl selenolate: An interesting “on water” nucleophilic reagent. Eur J Org Chem 2008; 2008(32): 5387-90.
[http://dx.doi.org/10.1002/ejoc.200800869]
[10]
Monti B, Santi C, Bagnoli L, Marini F, Sancineto L. Zinc chalcogenolates as green reagents. Curr Green Chem 2016; 3: 68-75.
[http://dx.doi.org/10.2174/2213346103666160127003716]
[11]
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.
[http://dx.doi.org/10.2174/2212796811307010003]
[12]
Santi C, Santoro S, Battistelli B. Organoselenium compounds as catalysts in nature and laboratory. Curr Org Chem 2010; 14: 2442-62.
[http://dx.doi.org/10.2174/138527210793358231]
[13]
Sancineto L, Mariotti A, Bagnoli L, Marini F, Desantis J, Iraci N, et al. Design and synthesis of diselenobisbenzamides (DISEBAS) as nucleocapsid protein 7 (ncp7) inhibitors with anti-HIV activity. J Med Chem 2015; 58(24): 9601-14.
[http://dx.doi.org/10.1021/acs.jmedchem.5b01183]
[14]
Jastrzebska, Mellea, Salerno, Grzes, Siergiejczyk, Niemirowicz-Laskowska-L, PhSeZnCl in the synthesis of steroidal β-hydroxy-phenylselenides having antibacterial activity. Int J Mol Sci 2019; 20(9): 2121.
[http://dx.doi.org/10.3390/ijms20092121]
[15]
Galant LS, Braga MM, de Souza D, de Bem AF, Sancineto L, Santi C, et al. Induction of reactive oxygen species by diphenyl diselenide is preceded by changes in cell morphology and permeability in Saccharomyces cerevisiae. Free Radic Res 2017; 51(7-8): 657-68.
[http://dx.doi.org/10.1080/10715762.2017.1355054]


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Article Details

VOLUME: 14
ISSUE: 2
Year: 2020
Page: [69 - 70]
Pages: 2
DOI: 10.2174/221279681402201119090048

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