2-ISOXAZOLINES WITH AN ELECTRON-ACCEPTOR SUBSTITUENT AT C(5) IN REACTIONS WITH NUCLEOPHILIC REAGENTS

Abstract

Depending on the substituent at position 5 of the  heterocycle, reaction of 2-isoxazolines with K-selectride, molybdenum hexacarbonyl, dimsyl sodium, and butyl lithium gave 1,3-cyclo-decomposition, aromatization of the isoxazoline ring, or reduction of the functional groups in the substituted isoxazolines.

How to Cite
Koroleva, E. V.; Bondar, N. F.; Katok, Ya. M.; Chekanov, N. A.; Chernikhova, T. V.  Chem. Heterocycl. Compd. 2007, 43, 362. [Khim. Geterotsikl. Soedin. 2007, 447.]

For this article in the English edition see DOI 10.1007/s10593-007-0053-6