SYNTHESIS AND CONFIGURATION OF 6-ARYLIDENE-2-FURFURYLIDENECYCLOHEXANONES

Authors

  • А. П. Кривенько N. G. Chernyshevskii Saratov State University, Saratov
  • А. А. Бугаев N. G. Chernyshevskii Saratov State University, Saratov
  • А. Г. Голиков N. G. Chernyshevskii Saratov State University, Saratov

DOI:

https://doi.org/10.1007/8365

Keywords:

6-arylidene-2-furfurylidenecyclohexanones, aromatic aldehydes, α, β-unsaturated ketones, 5-nitrofurfural, furfural, crotonic condensation

Abstract

6-Arylidene-2-furfurylidenecyclohexanones were obtained  by the condensation of cyclohexanone with aldehydes of the aromatic and furan series under  conditions of base or acid catalysis. The effect of substituents  in  the aromatic ring on the activityof  the initial aldehyde was studied. According to data from the IR spectra, the obtained ketones exist in the form of trans,trans isomers.

How to Cite
Kriven'ko, A. P.; Bugaev, A. A.; Golikov, A. G. Chem. Heterocycl. Compd. 2005, 41, 163. [Khim. Geterotsikl. Soedin. 2005, 191.]

For this article in the English edition, see DOI 10.1007/s10593-005-0120-9

 

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Published

2023-11-30

Issue

No. 2 (2005)

Section

Original Papers