90133-35-0Relevant academic research and scientific papers
Room-Temperature Arylation of Thiols: Breakthrough with Aryl Chlorides
Jiang, Min,Li, Haifang,Yang, Haijun,Fu, Hua
, p. 874 - 879 (2017)
The formation of aryl C?S bonds is an important chemical transformation because aryl sulfides are valuable building blocks for the synthesis of biologically and pharmaceutically active molecules and organic materials. Aryl sulfides have traditionally been synthesized through the transition-metal-catalyzed cross-coupling of aryl halides with thiols. However, the aryl halides used are usually bromides and iodides; readily available, low-cost aryl chlorides often not reactive enough. Furthermore, the deactivation of transition-metal catalysts by thiols has forced chemists to use high catalyst loadings, specially designed ligands, high temperatures, and/or strong bases, thus leading to high costs and the incompatibility of some functional groups. Herein, we describe a simple and efficient visible-light photoredox arylation of thiols with aryl halides at room temperature. More importantly, various aryl chlorides are also effective arylation reagents under the present conditions.
Novel Rearrangement of 1,4-Ylidic Thiaanthracenes
Ohno, Sachio,Shimizu, Hiroshi,Kataoka, Tadashi,Hori, Mikio
, p. 2472 - 2478 (2007/10/02)
A novel rearrangement of 10-alkyl-9-aryl-10-thiaanthracenes is described. 9-Mesityl-10-methyl-10-thiaanthracene (8a) generated by proton abstraction of 9-mesityl-10-methylthioxanthenium perchlorate (7a) with sodium hydride in THF underwent thermal rearran
