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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Autores principales: Gelabert, L.I., Fascio, M.L., D'Accorso, N.B.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_0022152X_v40_n2_p341_Gelabert
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spelling todo:paper_0022152X_v40_n2_p341_Gelabert2023-10-03T14:27:48Z Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline Gelabert, L.I. Fascio, M.L. D'Accorso, N.B. 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 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. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_0022152X_v40_n2_p341_Gelabert
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic 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
spellingShingle 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
Gelabert, L.I.
Fascio, M.L.
D'Accorso, N.B.
Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
topic_facet 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
description 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.
format JOUR
author Gelabert, L.I.
Fascio, M.L.
D'Accorso, N.B.
author_facet Gelabert, L.I.
Fascio, M.L.
D'Accorso, N.B.
author_sort Gelabert, L.I.
title Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
title_short Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
title_full Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
title_fullStr Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
title_full_unstemmed Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
title_sort characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline
url http://hdl.handle.net/20.500.12110/paper_0022152X_v40_n2_p341_Gelabert
work_keys_str_mv AT gelabertli characterizationandidentificationofcleavageproductsof3glycosyl5substituted2isoxazoline
AT fascioml characterizationandidentificationofcleavageproductsof3glycosyl5substituted2isoxazoline
AT daccorsonb characterizationandidentificationofcleavageproductsof3glycosyl5substituted2isoxazoline
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