2-Isoxazolines with an electron-acceptor substituent at C(5) in reactions with nucleophilic reagents |
| |
| Authors: | E. V. Koroleva N. F. Bondar Ya. M. Katok N. A. Chekanov T. V. Chernikhova |
| |
| Affiliation: | (1) Institute of the Chemistry of New Materials, Belarus National Academy of Sciences, Minsk, 220141;(2) Belorussian Agricultural Technological University, Minsk, 220050;(3) Belorussian State Technological University, Minsk, 220050 |
| |
| 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. __________ Translated from Khimiya Geterotsiklicheskikh Soedinenii, No.3, 447–455, March, 2007. |
| |
| Keywords: | derivatives of 2-isoxazoline dimsyl sodium molybdenum hexacarbonyl K-selectride cyclodecomposition |
| 本文献已被 SpringerLink 等数据库收录！ |
|
