61081-33-2Relevant articles and documents
Copper-Mediated Decarboxylative Sulfonylation of Arylacetic Acids with Sodium Sulfinates
Wu, Yinrong,Chen, Jiewen,Li, Lu,Wen, Kangmei,Yao, Xingang,Pang, Jianxin,Wu, Ting,Tang, Xiaodong
supporting information, p. 7164 - 7168 (2020/10/02)
Herein, we present a copper-mediated decarboxylative sulfonylation of arylacetic acids with sodium sulfinates that provides viable access to sulfone compounds. This protocol features readily available feedstocks, simple operations, high regioselectivities, and moderate to good yields. The newly obtained products could be converted to other useful compounds. Importantly, the products and their derivatives exhibited potent antitumor activities in vitro, which were tested by MTT assay.
Synthesis of 2-aryl-3-arylsulfonylindoles and 2-anilino-3- arylsulfonylindoles from 2-(arylsulfonyl)methylanilines using the aza-Wittig reaction of iminophosphoranes
Takahashi, Masahiko,Suga, Daishi
, p. 986 - 990 (2007/10/03)
2-(Arylsulfonyl)methyl-N-(triphenylphosphoranylidene)-anilines 5 were prepared starting from 2-(arylsulfonyl)-methylanilines 2. The aza-Wittig reaction of iminophosphoranes 5 with acyl cyanides gave N- [aryl(cyano)methylene]-2-(arylsulfonyl)methylanilines
A simple and rapid preparation of sulfones from alkyl halides using ultrasound
Biswas,Jash,Bhattacharyya
, p. 491 - 492 (2007/10/02)
Appropriate alkyl halides and sodium p-toluenesulfinates react rapidly in DMF-water at room temperature under the influence of ultrasound to afford sulfones. Using this procedure a wide variety of sulfones have been prepared.