COMPOSITION OF REDUCTIVE CLEAVAGE PRODUCTS OF CYCLOPENTA[<i>d</i>]ISOXAZOLINES

Authors

  • И. П. Антоневич Institute of Bioorganic Chemistry, National Academy of Sciences of the Republic of Belarus, Minsk 220141

Keywords:

acyl cyclopentanes, isoxazolines, Raney nickel, prostanoids, reduction

Abstract

The composition of the reductive cleavage products of cyclopenta[d]isoxazolines in acid medium depends on the acid, Raney nickel, and solvent used. Depending on the reaction conditions, we obtained β-hydroxy ketones, α,β-unsaturated ketones, or 2-acylcyclopentanes as the major products.

How to Cite
Antonevich, I. P. Chem. Heterocycl. Compd. 2003, 39, 1355. [Khim. Geterotsikl. Soedin. 2003, 1538.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000010652.62741.f4

Published

2003-10-25

Issue

Section

Original Papers