Friedel−Crafts Arylation Reactions of <i>N</i>-Sulfonyl Aldimines or Sulfonamidesulfones with Electron-Rich Arenes Catalyzed by FeCl<sub>3</sub>·6H<sub>2</sub>O: Synthesis of Triarylmethanes and Bis-heteroarylarylmethanes
作者:Ponnaboina Thirupathi、Sung Soo Kim
DOI:10.1021/jo1010137
日期:2010.8.6
The FeCl3 center dot 6H(2)O-catalyzed Friedel-Crafts arylation reactions of N-sulfonyl aldimines or sulfonamidesulfones with electron-rich arenes and heteroarenes, which lead to the formation of triarylmethanes and bis-heteroarylarylmethanes, are developed. The use of mild reaction conditions, low catalytic loading, high yield, and single step synthesis are the advantages of the present procedure.
Novel and highly efficient one pot protocol for the synthesis of diversely functionalized triarylmethanes
作者:B. Madhu Babu、Pramod B. Thakur、Vikas M. Bangade、H.M. Meshram
DOI:10.1016/j.tetlet.2014.11.139
日期:2015.2
efficient, convenient, and novel one pot approach is described for the synthesis of triarylmethanes by in situ oxidation of benzylalcohols followed by the Friedel–Crafts alkylation of di/trimethoxybenzenes in the presence of BF3·OEt2. The generality of the present method is strengthened by screening a variety of aromatic, aliphatic, and heteroaromatic alcohols with methoxy arenes. Shorter reaction time