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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/2119
Ver los metadatos del registro completo
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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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1844614124646957056 |
score |
13.069144 |