99366-73-1Relevant academic research and scientific papers
Trisulfides over disulfides: Highly selective synthetic strategies, anti-proliferative activities and sustained H2S release profiles
Bhattacherjee, Debojit,Sufian, Abu,Mahato, Sulendar K.,Begum, Samiyara,Banerjee, Kaustav,De, Sharmistha,Srivastava, Hemant Kumar,Bhabak, Krishna P.
supporting information, p. 13534 - 13537 (2019/11/14)
Temperature-and solvent-induced selective synthesis of trisulfides and disulfides is demonstrated. A remarkable selectivity was achieved using Na2S 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 H2S and potent anti-cancer activities.
Synthesis of a photocontrollable hydrogen sulfide donor using ketoprofenate photocages
Fukushima, Naoki,Ieda, Naoya,Sasakura, Kiyoshi,Nagano, Tetsuo,Hanaoka, Kenjiro,Suzuki, Takayoshi,Miyata, Naoki,Nakagawa, Hidehiko
supporting information, p. 587 - 589 (2014/01/06)
We report the design, synthesis and application of a directly photocontrollable hydrogen sulfide (H2S) donor, which releases H 2S proportionally to the intensity and duration of photoirradiation. Photocontrolled H2S releas
L'o-nitrobenzylidenedimethylsulfuranne: synthese, reactivite
Stanc, Yannick Le,Corre, Maurice Le
, p. 2958 - 2960 (2007/10/02)
In aqueous solution, o-nitrobenzyldimethylsulfonium bromide and the corresponding ylid give, depending upon the conditions, o-nitrobenzyl alcohol, o-nitrobenzylsulfide, or methyl o-hydroxymethylbenzyl sulfide.The o-nitrophenyloxiranes may be obtained by the reaction of nitrobenzylidenedimethylsulfurane with aldehydes in a two-phase aqueous sodium hydroxide/dichloromethane system.
