SYNTHESIS OF QUINOLIN-2-ONES BY AN INTRAMOLECULAR KNOEVENAGEL CONDENSATION AND BY TANDEM MICHAEL-KNOEVENAGEL HETEROCYCLIZATION

Authors

  • С. С. Мочалов M. V. Lomonosov Moscow State University
  • М. И. Хасанов M. V. Lomonosov Moscow State University
  • А. Н. Федотов M. V. Lomonosov Moscow State University
  • Н. С. Зефиров M. V. Lomonosov Moscow State University

DOI:

https://doi.org/10.1007/1394

Keywords:

acyl-2-(N-acylamino)benzenes, acyl-2-vinylcarbonylaminobenzenes, quinolin-2-ones, intramolecular Knoevenagel condensation, tandem heterocyclization

Abstract

The synthesis of 2-(N-R-amino)- and 2-(N-vinylcarbonylamino)acylbenzenes has been carried out and their heterocyclization into quinolin-2-ones under the action of sodium ethylate has been studied.

Authors: S. S. Mochalov, M. I. Chasanov, A. N. Fedotov, and N. S. Zefirov.

English translation in Chemistry of Heterocyclic Compounds, 2011, 47 (9), pp 1105-1121

http://link.springer.com/article/10.1007/s10593-011-0881-2

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Published

2013-12-17

Issue

No. 9 (2011)

Section

Original Papers