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Synthesis of Aminobismuthanes via Me 3 SnCl Elimination
Author(s) -
Schulz Axel,
Thomas Max,
Villinger Alexander
Publication year - 2017
Publication title -
zeitschrift für anorganische und allgemeine chemie
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.354
H-Index - 66
eISSN - 1521-3749
pISSN - 0044-2313
DOI - 10.1002/zaac.201700162
Subject(s) - chemistry , steric effects , medicinal chemistry , stereochemistry
The synthesis of N ‐trimethylstannylamines of the type R N(SnMe 3 )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 BiCl 3 leading to the formation of R N(H)BiCl 2 (for R = Ter), ( R NH) 3 Bi (for R = Mes*), and R N(BiCl 2 ) 2 (for R = Ar*). The synthesis and structure of the starting material R N(SnMe 3 )H and the new aminobismuthanes are reported.

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