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.
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REFERENCES
F. A. Lakhvich andE. V. Koroleva, Zh. Org. Khim., 35, 1749 (1999).
F. A. Lakhvich,V. A. Khripach,I. P. Antonevich,T. V. Yankova,E. V. Koroleva, andA. A. Akhrem, Khim. Geterotsikl. Soedin., 966 (1988).
I. P. Antonevich andF. A. Lakhvich, Zh. Org. Khim., 34, 718 (1998).
D. P. Curran andC. J. Fenk, Tetrahedron Lett., 27, 4865 (1986).
Organicum [Russian translation], Mir, Moscow (1992); 2, p. 419.
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Antonevich, I.P. Composition of Reductive Cleavage Products of Cyclopenta[d]isoxazolines. Chemistry of Heterocyclic Compounds 39, 1355–1356 (2003). https://doi.org/10.1023/B:COHC.0000010652.62741.f4
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DOI: https://doi.org/10.1023/B:COHC.0000010652.62741.f4