Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses

Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.

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Detalles Bibliográficos
Autores principales: D'Accorso, N.B., Thiel, I.M.E.
Formato: JOUR
Materias:
Nuclear magnetic resonance
Synthesis (chemical)
Acyclic monosaccharides
C NMR data
Monosaccharide synthesis
Glucose
disaccharide
article
carbohydrate analysis
carbohydrate synthesis
nuclear magnetic resonance
Carbohydrate Conformation
Carbohydrate Sequence
Comparative Study
Disaccharides
Indicators and Reagents
Magnetic Resonance Spectroscopy
Molecular Sequence Data
Molecular Structure
Structure-Activity Relationship
Support, Non-U.S. Gov't
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00086215_v245_n1_p145_DAccorso
Aporte de:
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires
id todo:paper_00086215_v245_n1_p145_DAccorso
record_format dspace
spelling todo:paper_00086215_v245_n1_p145_DAccorso2023-10-03T14:06:38Z Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses D'Accorso, N.B. Thiel, I.M.E. Nuclear magnetic resonance Synthesis (chemical) Acyclic monosaccharides C NMR data Monosaccharide synthesis Glucose disaccharide article carbohydrate analysis carbohydrate synthesis nuclear magnetic resonance Carbohydrate Conformation Carbohydrate Sequence Comparative Study Disaccharides Indicators and Reagents Magnetic Resonance Spectroscopy Molecular Sequence Data Molecular Structure Structure-Activity Relationship Support, Non-U.S. Gov't Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Thiel, I.M.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00086215_v245_n1_p145_DAccorso
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Nuclear magnetic resonance
Synthesis (chemical)
Acyclic monosaccharides
C NMR data
Monosaccharide synthesis
Glucose
disaccharide
article
carbohydrate analysis
carbohydrate synthesis
nuclear magnetic resonance
Carbohydrate Conformation
Carbohydrate Sequence
Comparative Study
Disaccharides
Indicators and Reagents
Magnetic Resonance Spectroscopy
Molecular Sequence Data
Molecular Structure
Structure-Activity Relationship
Support, Non-U.S. Gov't
spellingShingle Nuclear magnetic resonance
Synthesis (chemical)
Acyclic monosaccharides
C NMR data
Monosaccharide synthesis
Glucose
disaccharide
article
carbohydrate analysis
carbohydrate synthesis
nuclear magnetic resonance
Carbohydrate Conformation
Carbohydrate Sequence
Comparative Study
Disaccharides
Indicators and Reagents
Magnetic Resonance Spectroscopy
Molecular Sequence Data
Molecular Structure
Structure-Activity Relationship
Support, Non-U.S. Gov't
D'Accorso, N.B.
Thiel, I.M.E.
Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
topic_facet Nuclear magnetic resonance
Synthesis (chemical)
Acyclic monosaccharides
C NMR data
Monosaccharide synthesis
Glucose
disaccharide
article
carbohydrate analysis
carbohydrate synthesis
nuclear magnetic resonance
Carbohydrate Conformation
Carbohydrate Sequence
Comparative Study
Disaccharides
Indicators and Reagents
Magnetic Resonance Spectroscopy
Molecular Sequence Data
Molecular Structure
Structure-Activity Relationship
Support, Non-U.S. Gov't
description Fil:D'Accorso, N.B. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina.
format JOUR
author D'Accorso, N.B.
Thiel, I.M.E.
author_facet D'Accorso, N.B.
Thiel, I.M.E.
author_sort D'Accorso, N.B.
title Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
title_short Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
title_full Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
title_fullStr Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
title_full_unstemmed Synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-O-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
title_sort synthesis and characterization of two 1,2,3,6,2′,3′,4′,6′-octa-o-benzoyl-β-d-hexapyranosyl-(1 → 4)β-d-allopyranoses
url http://hdl.handle.net/20.500.12110/paper_00086215_v245_n1_p145_DAccorso
work_keys_str_mv AT daccorsonb synthesisandcharacterizationoftwo12362346octaobenzoylbdhexapyranosyl14bdallopyranoses
AT thielime synthesisandcharacterizationoftwo12362346octaobenzoylbdhexapyranosyl14bdallopyranoses
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