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...

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Detalles Bibliográficos
Autores principales: Gelabert, L.I., Fascio, M.L., D'Accorso, N.B.
Formato: JOUR
Materias:
aliphatic compound
aromatic compound
chemical compound
heterocyclic compound
isoxazoline derivative
article
carbon nuclear magnetic resonance
physical chemistry
protein analysis
protein degradation
proton nuclear magnetic resonance
spectroscopy
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_0022152X_v40_n2_p341_Gelabert
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
Descripción
Sumario: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 physically and spectroscopically.

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