Trisulfides over disulfides: highly selective synthetic strategies, anti-proliferative activities and sustained HS 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 (9), p.13534-13537 |
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| container_end_page | 13537 |
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| container_issue | 9 |
| container_start_page | 13534 |
| 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.
Highly selective synthesis of trisulfides over disulfides is demonstrated along with their potential as anti-proliferative agents and sustained donors of H
2
S. |
| doi_str_mv | 10.1039/c9cc05562b |
| format | Article |
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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.
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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.
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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.
Highly selective synthesis of trisulfides over disulfides is demonstrated along with their potential as anti-proliferative agents and sustained donors of H
2
S.</abstract><doi>10.1039/c9cc05562b</doi><tpages>4</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2019-11, Vol.55 (9), p.13534-13537 |
| issn | 1359-7345 1364-548X |
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| recordid | cdi_rsc_primary_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 HS release profiles |
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