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NaClO-Promoted Atroposelective Couplings of 3-Substituted Indoles with Amino Acid Derivatives
A new class of C-N axial chirality based on N-indole sulfonamides has been disclosed. This new axially chiral N-indole sulfonamides were constructed by NaClO-promoted couplings of 3-substituted indoles with chiral amino acid-based sulfonamides. A series of structurally diverse N-indole sulfonamide-based atropisomers were prepared using this established method. The stability of these structurally interesting atropisomers highly relied on the C3-substituents of indoles and side chains of amino acid derivatives.
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Reference:
Indole alkaloid derivatives as building blocks of natural products from?Bacillus thuringiensis?and?Bacillus velezensis?and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles