Trisulfides over disulfides: highly selective synthetic strategies, anti-proliferative activities and sustained H 2 S release profiles
Temperature- and solvent-induced selective synthesis of trisulfides and disulfides is demonstrated. A remarkable selectivity was achieved using Na 2 S as a sulfur-transfer agent under mild, greener, catalyst-free and additive-free conditions. This study reveals trisulfides as a better model than dis...
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2019-11, Vol.55 (90), p.13534-13537 |
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| container_issue | 90 |
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| container_title | Chemical communications (Cambridge, England) |
| container_volume | 55 |
| creator | Bhattacherjee, Debojit Sufian, Abu Mahato, Sulendar K. Begum, Samiyara Banerjee, Kaustav De, Sharmistha Srivastava, Hemant Kumar Bhabak, Krishna P. |
| description | Temperature- and solvent-induced selective synthesis of trisulfides and disulfides is demonstrated. A remarkable selectivity was achieved using Na
2
S as a sulfur-transfer agent under mild, greener, catalyst-free and additive-free conditions. This study reveals trisulfides as a better model than disulfides in general for a sustained release of H
2
S and potent anti-cancer activities. |
| doi_str_mv | 10.1039/C9CC05562B |
| format | Article |
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| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2019-11, Vol.55 (90), p.13534-13537 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_crossref_primary_10_1039_C9CC05562B |
| source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| title | Trisulfides over disulfides: highly selective synthetic strategies, anti-proliferative activities and sustained H 2 S release profiles |
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