67438-07-7Relevant academic research and scientific papers
Thioesters as Bifunctional Reagents for 2-Naphthylamine Sulfuracylation
Xiao, Fuhong,Yuan, Shanshan,Wang, Dahan,Liu, Saiwen,Huang, Huawen,Deng, Guo-Jun
, p. 3331 - 3336 (2019)
An efficient and convenient strategy for the preparation of diaryl sulfides via a Fe-promoted direct sulfuracylation of 2-naphthylamine using thioesters as bifunctional reagents is described. This synthetic strategy features high chemoselectivity, good substrate scope and functional group tolerance. (Figure presented.).
Synthesis of a benzenethiol-derivatized porphyrin for self-assembly
Wan, Jicheng,Sun, Huiqian,Huang, Xuebin
, p. 1841 - 1844 (2012/10/29)
The synthesis of a benzenethiol-derivatized porphyrin for flat-lying self-assembly on gold substrates is described. Acetyl protected thiol is not stable enough in Pd-catalyzed reactions. While acrylate derivatives protected thiol group shows good tolerance in Pd-catalyzed borylations and Suzuki-Miyaura coupling reactions and no catalyst poisoning was observed.
Electric Current through a Molecular Rod - Relevance of the Position of the Anchor Groups
Mayor, Marcel,Weber, Heiko B.,Reichert, Joachim,Elbing, Mark,Von Haenisch, Carsten,Beckmann, Detlef,Fischer, Matthias
, p. 5834 - 5838 (2007/10/03)
The electronic resistance of an electrode-molecule-electrode device strongly depends on the relative position of the anchor group in the molecular structure. The molecular rod, immobilized through two sulfur groups in the meta position on a pair of electr
