3 years ago

Synthesis of Aminobismuthanes via Me3SnCl Elimination

Synthesis of Aminobismuthanes via Me3SnCl Elimination
Max Thomas, Alexander Villinger, Axel Schulz
The synthesis of N-trimethylstannylamines of the type RN(SnMe3)H (stannylated anilines) with the sterically encumbered substituents R such as Ter [terphenyl, 2,6-bis(2,4,6-trimethylphenyl)-phenyl], Ar* [2,6-bis(diphenylmethyl)-4-methylphenyl], and Mes* (supermesityl, 2,4,6-tri-tert-butylphenyl) is described. These stannylated anilines were treated with BiCl3 leading to the formation of RN(H)BiCl2 (for R = Ter), (RNH)3Bi (for R = Mes*), and RN(BiCl2)2 (for R = Ar*). The synthesis and structure of the starting material RN(SnMe3)H and the new aminobismuthanes are reported.

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/zaac.201700162

You might also like
Discover & Discuss Important Research

Keeping up-to-date with research can feel impossible, with papers being published faster than you'll ever be able to read them. That's where Researcher comes in: we're simplifying discovery and making important discussions happen. With over 19,000 sources, including peer-reviewed journals, preprints, blogs, universities, podcasts and Live events across 10 research areas, you'll never miss what's important to you. It's like social media, but better. Oh, and we should mention - it's free.

  • Download from Google Play
  • Download from App Store
  • Download from AppInChina

Researcher displays publicly available abstracts and doesn’t host any full article content. If the content is open access, we will direct clicks from the abstracts to the publisher website and display the PDF copy on our platform. Clicks to view the full text will be directed to the publisher website, where only users with subscriptions or access through their institution are able to view the full article.