SYNTHESIS OF SUBSTITUTED HEXAHYDROINDAZOLES

Authors

  • А. А. Бугаев N. G. Chernyshevskii Saratov State University, Saratov 410601
  • А. Г. Голиков N. G. Chernyshevskii Saratov State University, Saratov 410601
  • А. П. Кривенько N. G. Chernyshevskii Saratov State University, Saratov 410601

DOI:

https://doi.org/10.1007/8237

Keywords:

6-arylidene-2-furfurylidenecyclohexanones, hydrazines, indazoles, α, β-unsaturated ketones, heterocyclization

Abstract

Substituted hexahydroindazoles were obtained by the reaction of 6-arylidene-2-furfurylidene-cyclohexanones with phenylhydrazine. It was concluded by means of the NMR spectra that azacyclization takes place regioselectively with participation of the arylidenecyclohexanone fragment.

How to Cite
Bugaev, A. A.; Golikov, A. G.; Kriven'ko, A. P.  Chem. Heterocycl. Compd. 2005, 41, 1. [Khim. Geterotsikl. Soedin. 2005, 1.]

For this article in the English edition, see DOI 10.1007/s10593-005-0233-1


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Published

2023-10-31

Issue

No. 7 (2005)

Section

Original Papers