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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2003
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| 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 |
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paper:paper_0022152X_v40_n2_p341_Gelabert2023-06-08T14:46:49Z Characterization and identification of cleavage products of 3-glycosyl-5-substituted-2-isoxazoline 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. 2003 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 |
| 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 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. |
| 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 |
| publishDate |
2003 |
| url |
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 |
| _version_ |
1768546753048477696 |