Issue 77, 2014

Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles

Abstract

Asymmetric N-alkylations of isatins with enals were shown to be feasible via a prolinol-catalyzed iminium activation, and N-alkylated isatins were obtained in good yields and with excellent enantioselectivity. The biologically useful N-alkylated isatins also served as valuable synthetic precursors, and could be readily converted to chiral N-alkylated indole derivatives. The described method provides a novel entry to access optically enriched N-alkylated isatins and indole derivatives.

Graphical abstract: Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles

Supplementary files

Article information

Article type
Communication
Submitted
17 Jun 2014
Accepted
01 Aug 2014
First published
01 Aug 2014

Chem. Commun., 2014,50, 11354-11357

Author version available

Enantioselective N-alkylation of isatins and synthesis of chiral N-alkylated indoles

X. Dou, W. Yao, C. Jiang and Y. Lu, Chem. Commun., 2014, 50, 11354 DOI: 10.1039/C4CC04586F

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