REDUCTION OF DERIVATIVES OF α-ARYLIDENE-α-(2-THIAZOLYL)ACETONITRILE WITH LITHIUM ALUMINUM HYDRIDE

Authors

  • А. А. Зубарев N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 119991
  • В. К. Завьялова N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 119991
  • В. П. Литвинов N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 119991

DOI:

https://doi.org/10.1007/8371

Keywords:

α-arylidene-α-(2-thiazolyl)acetonitriles, β-arylidene-β-(2-thiazolyl)ethylamines, lithium aluminum hydride, reduction

Abstract

The action of lithium aluminum hydride on derivatives of  α-arylidene-α-(2-thiazolyl)acetonitrile in absolute ether leads to reduction of the nitrile group without affecting the double bond conjugated with it. The reaction products are the corresponding substituted allylamines.

How to Cite
Zubarev, A. A.; Zav'yalova, V. K.; Litvinov, V. P. Chem. Heterocycl. Compd. 2005, 41, 192. [Khim. Geterotsikl. Soedin. 2005, 221.]

For this article in the English edition, see DOI 10.1007/s10593-005-0126-3


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Published

2023-11-30

Issue

No. 2 (2005)

Section

Original Papers