Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre

Autores
Colomer, Juan Pablo; Manzano, Veronica Elena; Varela, Oscar Jose
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The oxidation of per-O-acetyl (1,3)- and (1,4)-linked thiodisaccharides containing glucose, gulose and galactose residues, with an excess of m-chloroperbenzoic acid afforded the corresponding sulfoxides or sulfones. The latter were formed when the oxidation reaction was conducted for longer times. The sulfoxides were obtained as diastereomeric mixtures due to the chirality of the sulfur atom. Both diastereoisomers of the (1,3)-thiodisaccharides S-oxides were isolated by column chromatography, while the S-(1,4)-linked analogues could not be separated. The absolute configuration of the sulfur stereocenter of sulfoxides was assigned using NMR spectroscopy and taking into account the preferred conformations of the molecules and the shielding/deshielding of proton signals caused by anisotropy of the S=O bond and related effects. Most of the thiodisaccharide S-oxides were successfully O-deacetylated with MeOH-Et3N-H2O, whereas the sulfone underwent elimination reactions. Therefore, the oxidation was performed on the free thiodisaccharides, and the corresponding sulfones were obtained in very good yields.
Fil: Colomer, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
Fil: Manzano, Veronica Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
Fil: Varela, Oscar Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
Materia
Glycosyl Sulfoxide
Glycosyl Sulfone
Sulfur Stereocenter
Sulfoxide Configuration
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/2119

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spelling Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur StereocentreColomer, Juan PabloManzano, Veronica ElenaVarela, Oscar JoseGlycosyl SulfoxideGlycosyl SulfoneSulfur StereocenterSulfoxide Configurationhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The oxidation of per-O-acetyl (1,3)- and (1,4)-linked thiodisaccharides containing glucose, gulose and galactose residues, with an excess of m-chloroperbenzoic acid afforded the corresponding sulfoxides or sulfones. The latter were formed when the oxidation reaction was conducted for longer times. The sulfoxides were obtained as diastereomeric mixtures due to the chirality of the sulfur atom. Both diastereoisomers of the (1,3)-thiodisaccharides S-oxides were isolated by column chromatography, while the S-(1,4)-linked analogues could not be separated. The absolute configuration of the sulfur stereocenter of sulfoxides was assigned using NMR spectroscopy and taking into account the preferred conformations of the molecules and the shielding/deshielding of proton signals caused by anisotropy of the S=O bond and related effects. Most of the thiodisaccharide S-oxides were successfully O-deacetylated with MeOH-Et3N-H2O, whereas the sulfone underwent elimination reactions. Therefore, the oxidation was performed on the free thiodisaccharides, and the corresponding sulfones were obtained in very good yields.Fil: Colomer, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;Fil: Manzano, Veronica Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;Fil: Varela, Oscar Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;Wiley VCH Verlag2013-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/2119Colomer, Juan Pablo; Manzano, Veronica Elena; Varela, Oscar Jose; Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre; Wiley VCH Verlag; European Journal of Organic Chemistry; 2013; 32; 11-2013; 7343-73531434-193Xenginfo:eu-repo/semantics/altIdentifier/doi/DOI:10.1002/ejoc.201301037info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201301037/abstractinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:17:15Zoai:ri.conicet.gov.ar:11336/2119instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:17:16.169CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
title Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
spellingShingle Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
Colomer, Juan Pablo
Glycosyl Sulfoxide
Glycosyl Sulfone
Sulfur Stereocenter
Sulfoxide Configuration
title_short Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
title_full Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
title_fullStr Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
title_full_unstemmed Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
title_sort Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre
dc.creator.none.fl_str_mv Colomer, Juan Pablo
Manzano, Veronica Elena
Varela, Oscar Jose
author Colomer, Juan Pablo
author_facet Colomer, Juan Pablo
Manzano, Veronica Elena
Varela, Oscar Jose
author_role author
author2 Manzano, Veronica Elena
Varela, Oscar Jose
author2_role author
author
dc.subject.none.fl_str_mv Glycosyl Sulfoxide
Glycosyl Sulfone
Sulfur Stereocenter
Sulfoxide Configuration
topic Glycosyl Sulfoxide
Glycosyl Sulfone
Sulfur Stereocenter
Sulfoxide Configuration
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv The oxidation of per-O-acetyl (1,3)- and (1,4)-linked thiodisaccharides containing glucose, gulose and galactose residues, with an excess of m-chloroperbenzoic acid afforded the corresponding sulfoxides or sulfones. The latter were formed when the oxidation reaction was conducted for longer times. The sulfoxides were obtained as diastereomeric mixtures due to the chirality of the sulfur atom. Both diastereoisomers of the (1,3)-thiodisaccharides S-oxides were isolated by column chromatography, while the S-(1,4)-linked analogues could not be separated. The absolute configuration of the sulfur stereocenter of sulfoxides was assigned using NMR spectroscopy and taking into account the preferred conformations of the molecules and the shielding/deshielding of proton signals caused by anisotropy of the S=O bond and related effects. Most of the thiodisaccharide S-oxides were successfully O-deacetylated with MeOH-Et3N-H2O, whereas the sulfone underwent elimination reactions. Therefore, the oxidation was performed on the free thiodisaccharides, and the corresponding sulfones were obtained in very good yields.
Fil: Colomer, Juan Pablo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
Fil: Manzano, Veronica Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Instituto de Química, Física de los Materiales, Medioambiente y Energía; Argentina; Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
Fil: Varela, Oscar Jose. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Centro de Investigaciones en Hidratos de Carbono; Argentina;
description The oxidation of per-O-acetyl (1,3)- and (1,4)-linked thiodisaccharides containing glucose, gulose and galactose residues, with an excess of m-chloroperbenzoic acid afforded the corresponding sulfoxides or sulfones. The latter were formed when the oxidation reaction was conducted for longer times. The sulfoxides were obtained as diastereomeric mixtures due to the chirality of the sulfur atom. Both diastereoisomers of the (1,3)-thiodisaccharides S-oxides were isolated by column chromatography, while the S-(1,4)-linked analogues could not be separated. The absolute configuration of the sulfur stereocenter of sulfoxides was assigned using NMR spectroscopy and taking into account the preferred conformations of the molecules and the shielding/deshielding of proton signals caused by anisotropy of the S=O bond and related effects. Most of the thiodisaccharide S-oxides were successfully O-deacetylated with MeOH-Et3N-H2O, whereas the sulfone underwent elimination reactions. Therefore, the oxidation was performed on the free thiodisaccharides, and the corresponding sulfones were obtained in very good yields.
publishDate 2013
dc.date.none.fl_str_mv 2013-11
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/2119
Colomer, Juan Pablo; Manzano, Veronica Elena; Varela, Oscar Jose; Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre; Wiley VCH Verlag; European Journal of Organic Chemistry; 2013; 32; 11-2013; 7343-7353
1434-193X
url http://hdl.handle.net/11336/2119
identifier_str_mv Colomer, Juan Pablo; Manzano, Veronica Elena; Varela, Oscar Jose; Synthesis of Thiodisaccharide Sulfoxides and Sulfones – Determination of the Configuration of the Sulfur Stereocentre; Wiley VCH Verlag; European Journal of Organic Chemistry; 2013; 32; 11-2013; 7343-7353
1434-193X
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/DOI:10.1002/ejoc.201301037
info:eu-repo/semantics/altIdentifier/url/http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201301037/abstract
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley VCH Verlag
publisher.none.fl_str_mv Wiley VCH Verlag
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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