b-Diketones derived from cyclopentadienyl rhenium tricarbonyl

The acetyl complex (η5–C5H4COCH3)Re(CO)3 reacts with KOtBu and an excess of appropriate ester to provide cyrhetrenyl-β-diketones complexes (η5–C5H4COCH2COR)Re(CO)3 (R = CF3, 1a; CH3, 1b; Ph, 1c). These new 1,3-diketones exist predominantly as enol tautome

Detalles Bibliográficos
Autores: Cautivo, T., Godoy, F., Klahn, A. H., Buono-Core, G. E., Sierra, D., Fuentealba, M., Garland, M. T.
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2007
País:Chile
Idioma:inglés
OAI Identifier:oai:repositorio.anid.cl:10533/240695
Acceso en línea:https://hdl.handle.net/10533/240695
Access Level:acceso abierto
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spelling Garland, M. T.Fuentealba, M.Sierra, D.Buono-Core, G. E.Klahn, A. H.Godoy, F.Cautivo, T.200710.1016/j.inoche.2007.05.027https://hdl.handle.net/10533/240695http://purl.org/coar/access_right/c_abf2b-Diketones derived from cyclopentadienyl rhenium tricarbonylCautivo, T.Godoy, F.Klahn, A. H.Buono-Core, G. E.Sierra, D.Fuentealba, M.Garland, M. T.2020-03-11T20:35:37Z2022-07-08T17:11:04Z2020-03-11T20:35:37Z2022-07-08T17:11:04Z2007The acetyl complex (η5–C5H4COCH3)Re(CO)3 reacts with KOtBu and an excess of appropriate ester to provide cyrhetrenyl-β-diketones complexes (η5–C5H4COCH2COR)Re(CO)3 (R = CF3, 1a; CH3, 1b; Ph, 1c). These new 1,3-diketones exist predominantly as enol tautomeFONDAPFONDAP1198000211980002virtual::44541-1WOS:000249460300016https://hdl.handle.net/10533/240695eng10.1016/j.inoche.2007.05.027https://doi.org/10.1016/j.inoche.2007.05.027Atribución-NoComercial-SinDerivadas 3.0 Chilehttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/info:eu-repo/semantics/openAccessb-Diketones derived from cyclopentadienyl rhenium tricarbonylInorg. Chem. CommArticuloinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttps://hdl.handle.net/10533/240695FONDAPhttp://purl.org/coar/resource_type/c_2df8fbb19814cbeb-a770-4d7e-887e-3298f0f34a33virtual::44541-19814cbeb-a770-4d7e-887e-3298f0f34a33virtual::44541-110533/240695oai:repositorio.anid.cl:10533/2406952023-07-24 15:49:35.069https://repositorio.anid.clRepositorio ANIDaletelier@anid.cl
dc.title.none.fl_str_mv b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
dc.title.journal.none.fl_str_mv Inorg. Chem. Comm
title b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
spellingShingle b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
Cautivo, T.
title_short b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
title_full b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
title_fullStr b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
title_full_unstemmed b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
title_sort b-Diketones derived from cyclopentadienyl rhenium tricarbonyl
dc.creator.none.fl_str_mv Cautivo, T.
Godoy, F.
Klahn, A. H.
Buono-Core, G. E.
Sierra, D.
Fuentealba, M.
Garland, M. T.
author Cautivo, T.
author_facet Cautivo, T.
Godoy, F.
Klahn, A. H.
Buono-Core, G. E.
Sierra, D.
Fuentealba, M.
Garland, M. T.
author_role author
author2 Godoy, F.
Klahn, A. H.
Buono-Core, G. E.
Sierra, D.
Fuentealba, M.
Garland, M. T.
author2_role author
author
author
author
author
author
description The acetyl complex (η5–C5H4COCH3)Re(CO)3 reacts with KOtBu and an excess of appropriate ester to provide cyrhetrenyl-β-diketones complexes (η5–C5H4COCH2COR)Re(CO)3 (R = CF3, 1a; CH3, 1b; Ph, 1c). These new 1,3-diketones exist predominantly as enol tautome
publishDate 2007
dc.date.issued.none.fl_str_mv 2007
dc.date.accessioned.none.fl_str_mv 2020-03-11T20:35:37Z
2022-07-08T17:11:04Z
dc.date.available.none.fl_str_mv 2020-03-11T20:35:37Z
2022-07-08T17:11:04Z
dc.type.none.fl_str_mv Articulo
dc.type.driver.none.fl_str_mv info:eu-repo/semantics/article
dc.type.openaire.none.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.folio.none.fl_str_mv 11980002
11980002
dc.identifier.idwos.none.fl_str_mv WOS:000249460300016
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10533/240695
identifier_str_mv 11980002
WOS:000249460300016
url https://hdl.handle.net/10533/240695
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.doi.none.fl_str_mv 10.1016/j.inoche.2007.05.027
dc.relation.uri.none.fl_str_mv https://doi.org/10.1016/j.inoche.2007.05.027
dc.rights.none.fl_str_mv Atribución-NoComercial-SinDerivadas 3.0 Chile
http://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rights.driver.none.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv Atribución-NoComercial-SinDerivadas 3.0 Chile
http://creativecommons.org/licenses/by-nc-nd/3.0/cl/
eu_rights_str_mv openAccess
repository.name.fl_str_mv Repositorio ANID
repository.mail.fl_str_mv aletelier@anid.cl
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score 15,811543

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