40445-33-8Relevant academic research and scientific papers
Copper-catalyzed activation of disulfides as a key step in the synthesis of benzothiazole moieties
Hyvl, Jakub,Srogl, Jiri
supporting information; experimental part, p. 2849 - 2851 (2010/07/18)
A convenient synthesis of substituted benzothiazoles has been accomplished by way of a copper catalyzed reaction of aromatic disulfide amines and aldehydes. The process, which involves copper catalyzed activation of disulfide functionality, proceeds in a
Ascorbate mediated copper catalyzed reductive cross-coupling of disulfides with aryl iodides
Martinek, Marek,Korf, Michal,Srogl, Jiri
supporting information; experimental part, p. 4387 - 4389 (2010/08/06)
The concept of using ascorbic acid as a mediator/ reducing agent in a Cu(i) catalyzed process is introduced and further demonstrated on a cross-coupling reaction of aryl iodides with disulfides.
Shiga toxin-mediated retrograde delivery of a topoisomerase I inhibitor prodrug
El Alaoui, Abdessamad,Schmidt, Frederic,Amessou, Mohamed,Sarr, Marianne,Decaudin, Didier,Florent, Jean-Claude,Johannes, Ludger
, p. 6469 - 6472 (2008/09/17)
(Figure Presented) A retrograde strategy: An innovative cancer-cell delivery concept exploits the naturally evolved characteristics of the Shiga toxin B-subunit (STxB) for the intracellular activation of a newly synthesized prodrug at the level of the bio
