Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules
Benzyl β-d-galactofuranoside was efficiently obtained from 1,2,3,5,6-penta-O-benzoyl-α,β-d-galactofuranose, via benzyl 2,3,5,6-tetra-O-benzoyl-β-d-galactofuranoside. Conditions for the O-debenzylation were investigated in order to evaluate the synthetic application of the benzyl group as an anomeric...
Guardado en:
Autores principales: | , , |
---|---|
Formato: | JOUR |
Materias: | |
Acceso en línea: | http://hdl.handle.net/20.500.12110/paper_00086215_v341_n13_p2286_Marino |
Aporte de: |
id |
todo:paper_00086215_v341_n13_p2286_Marino |
---|---|
record_format |
dspace |
spelling |
todo:paper_00086215_v341_n13_p2286_Marino2023-10-03T14:07:10Z Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules Mariño, K. Baldoni, L. Marino, C. β-d-Galactofuranosides Benzyl galactofuranoside exo-β-d-Galactofuranosidase substrate Raney nickel Glucose Organic compounds Synthesis (chemical) β-d-Galactofuranosides Benzyl galactofuranoside Exo-β-d-Galactofuranosidase substrate Raney nickel Molecular structure 1,2,3,5,6 penta o benzoyl alpha,beta dextro galactofuranose benzyl 2,3,5,6 tetra o benzoyl beta dextro galactofuranoside beta dextro galactofuranoside dextro galactofuranose furan derivative unclassified drug article debenzylation priority journal synthesis Benzyl Compounds Carbohydrate Conformation Galactose Galactosides Molecular Structure Tetra Benzyl β-d-galactofuranoside was efficiently obtained from 1,2,3,5,6-penta-O-benzoyl-α,β-d-galactofuranose, via benzyl 2,3,5,6-tetra-O-benzoyl-β-d-galactofuranoside. Conditions for the O-debenzylation were investigated in order to evaluate the synthetic application of the benzyl group as an anomeric protector of a galactofuranose moiety in synthetic strategies involving galactofuranose. © 2006 Elsevier Ltd. All rights reserved. Fil:Mariño, K. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Baldoni, L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Marino, C. 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_v341_n13_p2286_Marino |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
β-d-Galactofuranosides Benzyl galactofuranoside exo-β-d-Galactofuranosidase substrate Raney nickel Glucose Organic compounds Synthesis (chemical) β-d-Galactofuranosides Benzyl galactofuranoside Exo-β-d-Galactofuranosidase substrate Raney nickel Molecular structure 1,2,3,5,6 penta o benzoyl alpha,beta dextro galactofuranose benzyl 2,3,5,6 tetra o benzoyl beta dextro galactofuranoside beta dextro galactofuranoside dextro galactofuranose furan derivative unclassified drug article debenzylation priority journal synthesis Benzyl Compounds Carbohydrate Conformation Galactose Galactosides Molecular Structure Tetra |
spellingShingle |
β-d-Galactofuranosides Benzyl galactofuranoside exo-β-d-Galactofuranosidase substrate Raney nickel Glucose Organic compounds Synthesis (chemical) β-d-Galactofuranosides Benzyl galactofuranoside Exo-β-d-Galactofuranosidase substrate Raney nickel Molecular structure 1,2,3,5,6 penta o benzoyl alpha,beta dextro galactofuranose benzyl 2,3,5,6 tetra o benzoyl beta dextro galactofuranoside beta dextro galactofuranoside dextro galactofuranose furan derivative unclassified drug article debenzylation priority journal synthesis Benzyl Compounds Carbohydrate Conformation Galactose Galactosides Molecular Structure Tetra Mariño, K. Baldoni, L. Marino, C. Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
topic_facet |
β-d-Galactofuranosides Benzyl galactofuranoside exo-β-d-Galactofuranosidase substrate Raney nickel Glucose Organic compounds Synthesis (chemical) β-d-Galactofuranosides Benzyl galactofuranoside Exo-β-d-Galactofuranosidase substrate Raney nickel Molecular structure 1,2,3,5,6 penta o benzoyl alpha,beta dextro galactofuranose benzyl 2,3,5,6 tetra o benzoyl beta dextro galactofuranoside beta dextro galactofuranoside dextro galactofuranose furan derivative unclassified drug article debenzylation priority journal synthesis Benzyl Compounds Carbohydrate Conformation Galactose Galactosides Molecular Structure Tetra |
description |
Benzyl β-d-galactofuranoside was efficiently obtained from 1,2,3,5,6-penta-O-benzoyl-α,β-d-galactofuranose, via benzyl 2,3,5,6-tetra-O-benzoyl-β-d-galactofuranoside. Conditions for the O-debenzylation were investigated in order to evaluate the synthetic application of the benzyl group as an anomeric protector of a galactofuranose moiety in synthetic strategies involving galactofuranose. © 2006 Elsevier Ltd. All rights reserved. |
format |
JOUR |
author |
Mariño, K. Baldoni, L. Marino, C. |
author_facet |
Mariño, K. Baldoni, L. Marino, C. |
author_sort |
Mariño, K. |
title |
Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
title_short |
Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
title_full |
Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
title_fullStr |
Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
title_full_unstemmed |
Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
title_sort |
facile synthesis of benzyl β-d-galactofuranoside. a convenient intermediate for the synthesis of d-galactofuranose-containing molecules |
url |
http://hdl.handle.net/20.500.12110/paper_00086215_v341_n13_p2286_Marino |
work_keys_str_mv |
AT marinok facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules AT baldonil facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules AT marinoc facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules |
_version_ |
1782023578978353152 |