PREPARATION OF CHIRAL PYRROLE DERIVATIVES BY THE PAAL-KNORR REACTION

Authors

  • И. О. Рыжков M. V. Lomonosov Moscow State University
  • И. А. Андреев M. V. Lomonosov Moscow State University
  • Г. М. Белов M. V. Lomonosov Moscow State University
  • А. В. Куркин M. V. Lomonosov Moscow State University
  • М. А. Юровская M. V. Lomonosov Moscow State University

DOI:

https://doi.org/10.1007/2133

Keywords:

1, 4-dicarbonyl compounds, 2, 5-dimethyl- and 5-aryl-2-methylpyrroles with a chiral substituent at the nitrogen atom, chiral pyrrole derivatives, iodine-catalyzed cyclization, Paal-Knorr method, Stetter reaction

Abstract

A new approach has been developed for the synthesis of N-alkylpyrroles with a chiral substituent at the nitrogen atom by the Paal-Knorr reaction using esters of amino acids as the source of chirality.

How to Cite
Ryzhkov, I. O.; Andreev, I. A.; Belov, G. M.; Kurkin, A. V.; Yurovskaya, M. A. Chem. Heterocycl. Compd. 2011, 47(2), 182. [Khim. Geterotsikl. Soedin. 2011, 231.]

For this article in the English edition see DOI 10.1007/s10593-011-0739-7

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Published

2014-12-04

Issue

No. 2 (2011)

Section

Original Papers