NEW STRATEGIES FOR THE SYNTHESIS OF <i>N</i>-ALKYLATED INDOLES

Authors

  • А. В. Карчава M. V. Lomonosov Moscow State University
  • Ф. С. Мелконян M. V. Lomonosov Moscow State University
  • М. А. Юровская M. V. Lomonosov Moscow State University

DOI:

https://doi.org/10.1007/1227

Keywords:

indole, natural compounds, aza-Michael reaction, Mitsunobu reaction, transition metal catalysis

Abstract

New data, mostly published in the last five years, on methods for the synthesis of N-alkylated indoles both as a result of direct introduction of the alkyl substituent at the nitrogen atom and by construction of the indole heterocyclic system are reviewed. Only examples of indole derivatives containing branched, sterically hindered, and chiral alkyl substituents at the nitrogen atom are discussed.

Authors: A. V. Karchava, F. S. Melkonyan, and M. A. Yurovskaya.

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (3), pp 391-407

http://link.springer.com/article/10.1007/s10593-012-1006-2

Published

2013-11-25

Issue

Section

Review Articles