Angewandte Chemie International Edition · 2004 · 131 citations · 22 references
Intramolecular CH insertion with sulfamates catalyzed by rhodium complexes offers an effective method for the preparation of N,O-acetals, which function as iminium ion precursors and undergo smooth diastereoselective coupling with nucleophiles under Lewis acidic conditions (see scheme). These findings advance the versatility of catalytic CH amination for the assembly of structurally complex nitrogen-containing products. Tf=trifluoromethanesulfonyl. Supporting information for this article is available on the WWW under http://www.wiley-vch.de/contents/jc_2002/2004/z460791_s.pdf or from the author. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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A Stereoselective Synthesis of (−)-Tetrodotoxin
A. Scott Hinman, J. Du Bois · Journal of the American Chemical Society · 2003 · 367 citations
Iminoiodanes and C-NBond Formation in Organic Synthesis
Philippe Dauban, Robert H. Dodd · Synlett · 2003 · 278 citations