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...

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Detalles Bibliográficos
Autores principales:	Mariño, Karina V., Baldoni, Luciana, Marino, María Carla
Publicado:	2006
Materias:	β-d-Galactofuranosides Benzyl galactofuranoside exo-β-d-Galactofuranosidase substrate Raney nickel Glucose Organic compounds Synthesis (chemical) Exo-β-d-Galactofuranosidase substrate 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
Acceso en línea:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v341_n13_p2286_Marino http://hdl.handle.net/20.500.12110/paper_00086215_v341_n13_p2286_Marino
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

id	paper:paper_00086215_v341_n13_p2286_Marino
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spelling	paper:paper_00086215_v341_n13_p2286_Marino2023-06-08T14:32:51Z Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules Mariño, Karina V. Baldoni, Luciana Marino, María Carla 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. 2006 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v341_n13_p2286_Marino 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, Karina V. Baldoni, Luciana Marino, María Carla 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.
author	Mariño, Karina V. Baldoni, Luciana Marino, María Carla
author_facet	Mariño, Karina V. Baldoni, Luciana Marino, María Carla
author_sort	Mariño, Karina V.
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
publishDate	2006
url	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v341_n13_p2286_Marino http://hdl.handle.net/20.500.12110/paper_00086215_v341_n13_p2286_Marino
work_keys_str_mv	AT marinokarinav facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules AT baldoniluciana facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules AT marinomariacarla facilesynthesisofbenzylbdgalactofuranosideaconvenientintermediateforthesynthesisofdgalactofuranosecontainingmolecules
_version_	1768542203169210368

Facile synthesis of benzyl β-d-galactofuranoside. A convenient intermediate for the synthesis of d-galactofuranose-containing molecules

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