A NEW REDOX SYSTEM: TRIСНLOROМETHYLARENE — PYRIDINE BASE

Authors

  • Leonid I. Belen'kii N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • Igor S. Poddubnyi N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • Mikhail М. Krayushkin N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow

Abstract

A redox reaction of trichloromethylarenes with pyridines results in respective N-(α-chloroarylmethyl)substituted pyridinium chlorides which give on hydrolysis aromatic aldehydes and 4-chloropyridines or 1,4'-bipyridinium salts.

How to Cite
Belen'kii, L. I.; Poddubnyi, I. S.; Krayushkin, M. M. Chem. Heterocycl. Compd. 1995, 31, 1201. [Khim. Geterotsikl. Soedin. 1995, 1373.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01185590

Published

1995-10-25

Issue

Section

Original Papers