Title of article
Dirhodium(II) tetrakis[N-tetrachlorophthaloyl-(S)-tert-leucinate]: a new chiral Rh(II) catalyst for enantioselective amidation of CH bonds
Author/Authors
Yamawaki، نويسنده , , Minoru and Tsutsui، نويسنده , , Hideyuki and Kitagaki، نويسنده , , Shinji and Anada، نويسنده , , Masahiro and Hashimoto، نويسنده , , Shunichi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2002
Pages
4
From page
9561
To page
9564
Abstract
Dirhodium(II) tetrakis[N-tetrachlorophthaloyl-(S)-tert-leucinate], characterized by substitution of chlorine atoms for four hydrogen atoms on the phthalimido group in the parent dirhodium(II) complex has been found to be well suited for enantioselective amidation of benzylic CH bonds with [(4-nitrophenyl)sulfonylimino]phenyliodinane. The observed enantioselectivity of up to 84% ee is the highest reported to date for dirhodium(II) complex-catalyzed CH amidations.
Journal title
Tetrahedron Letters
Serial Year
2002
Journal title
Tetrahedron Letters
Record number
1659715
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