Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
We report herein the synthesis of new synthons obtained by reductive opening of 3-glycosyl-5-substituted-2-isoxazolines. Different cleavage products have been obtained depending on the substituents (aliphatic or aromatic) in position five of the heterocycle ring. The new compounds are characterized...
Guardado en:
Publicado: |
2003
|
---|---|
Materias: | |
Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0022152X_v40_n2_p341_Gelabert http://hdl.handle.net/20.500.12110/paper_0022152X_v40_n2_p341_Gelabert |
Aporte de: |
Ejemplares similares
-
Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
por: Gelabert, L.I., et al. -
Synthesis, high-resolution NMR spectroscopic analysis, and single-crystal X-ray diffraction of isoxazoline tetracycles
Publicado: (2002) -
Synthesis, high-resolution NMR spectroscopic analysis, and single-crystal X-ray diffraction of isoxazoline tetracycles
por: Fascio, M.L., et al. -
Elucidation of the Average Molecular Structure of Argentinian Asphaltenes
por: Bava, Yanina Belén, et al.
Publicado: (2019) -
Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
por: Perissinotti, Laura L., et al.
Publicado: (2005)