Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process
- Autores
- Oksdath Mansilla, Gabriela; Argüello, Juan Elias; Peñeñory, Alicia Beatriz
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Aromatic and aliphatic ketones can be converted to methylene groups by desulfurization of the corresponding dithioketals in moderate to good yields. The reaction proceeds by photoinduced electron transfer from tert-BuOK in the presence of 1,4-dicyclohexadiene as hydrogen atom donor. The diene is able to trigger and keep a chain process by hydrogen transfer–proton transfer reactions.
Fil: Oksdath Mansilla, Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Argüello, Juan Elias. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
Fil: Peñeñory, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina - Materia
-
Carbonyl Reduction
Thioketals
Photochemistry
Electron Transfer - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/25017
Ver los metadatos del registro completo
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Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain processOksdath Mansilla, GabrielaArgüello, Juan EliasPeñeñory, Alicia BeatrizCarbonyl ReductionThioketalsPhotochemistryElectron Transferhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Aromatic and aliphatic ketones can be converted to methylene groups by desulfurization of the corresponding dithioketals in moderate to good yields. The reaction proceeds by photoinduced electron transfer from tert-BuOK in the presence of 1,4-dicyclohexadiene as hydrogen atom donor. The diene is able to trigger and keep a chain process by hydrogen transfer–proton transfer reactions.Fil: Oksdath Mansilla, Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Argüello, Juan Elias. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaFil: Peñeñory, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; ArgentinaElsevier2013-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/25017Oksdath Mansilla, Gabriela; Argüello, Juan Elias; Peñeñory, Alicia Beatriz; Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process; Elsevier; Tetrahedron Letters; 54; 12; 1-2013; 1515-15180040-4039CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2012.12.118info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403913000051info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:44:18Zoai:ri.conicet.gov.ar:11336/25017instacron: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:34982025-09-03 09:44:18.746CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
title |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
spellingShingle |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process Oksdath Mansilla, Gabriela Carbonyl Reduction Thioketals Photochemistry Electron Transfer |
title_short |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
title_full |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
title_fullStr |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
title_full_unstemmed |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
title_sort |
Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process |
dc.creator.none.fl_str_mv |
Oksdath Mansilla, Gabriela Argüello, Juan Elias Peñeñory, Alicia Beatriz |
author |
Oksdath Mansilla, Gabriela |
author_facet |
Oksdath Mansilla, Gabriela Argüello, Juan Elias Peñeñory, Alicia Beatriz |
author_role |
author |
author2 |
Argüello, Juan Elias Peñeñory, Alicia Beatriz |
author2_role |
author author |
dc.subject.none.fl_str_mv |
Carbonyl Reduction Thioketals Photochemistry Electron Transfer |
topic |
Carbonyl Reduction Thioketals Photochemistry Electron Transfer |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Aromatic and aliphatic ketones can be converted to methylene groups by desulfurization of the corresponding dithioketals in moderate to good yields. The reaction proceeds by photoinduced electron transfer from tert-BuOK in the presence of 1,4-dicyclohexadiene as hydrogen atom donor. The diene is able to trigger and keep a chain process by hydrogen transfer–proton transfer reactions. Fil: Oksdath Mansilla, Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Argüello, Juan Elias. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina Fil: Peñeñory, Alicia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina |
description |
Aromatic and aliphatic ketones can be converted to methylene groups by desulfurization of the corresponding dithioketals in moderate to good yields. The reaction proceeds by photoinduced electron transfer from tert-BuOK in the presence of 1,4-dicyclohexadiene as hydrogen atom donor. The diene is able to trigger and keep a chain process by hydrogen transfer–proton transfer reactions. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-01 |
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/11336/25017 Oksdath Mansilla, Gabriela; Argüello, Juan Elias; Peñeñory, Alicia Beatriz; Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process; Elsevier; Tetrahedron Letters; 54; 12; 1-2013; 1515-1518 0040-4039 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/25017 |
identifier_str_mv |
Oksdath Mansilla, Gabriela; Argüello, Juan Elias; Peñeñory, Alicia Beatriz; Photoreduction of aliphatic and aromatic thioketals: new access to the reduction of carbonyl groups by a desulfurization chain process; Elsevier; Tetrahedron Letters; 54; 12; 1-2013; 1515-1518 0040-4039 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2012.12.118 info:eu-repo/semantics/altIdentifier/url/http://www.sciencedirect.com/science/article/pii/S0040403913000051 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier |
publisher.none.fl_str_mv |
Elsevier |
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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1842268657019781120 |
score |
13.13397 |