Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride

Autores
Silveira, Claudio C.; Rinaldi, Francieli; Bassaco, Mariana M.; Kaufman, Teodoro Saul
Año de publicación
2010
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The NaH-promoted tandem Michael addition/intramolecular Wittig-Horner reaction of bis[(diphenylphosphinoyl) methyl]telluride with chalcones stereoselectively afforded trans-2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro- 2H-telluropyran derivatives in 51-72% yield, under mild conditions.
Fil: Silveira, Claudio C.. Universidade Federal de Santa Maria; Brasil
Fil: Rinaldi, Francieli. Universidade Federal de Santa Maria; Brasil
Fil: Bassaco, Mariana M.. Universidade Federal de Santa Maria; Brasil
Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
Materia
3,4-DIHYDRO-2H-TELLUROPYRANS
TANDEM REACTIONS
VINYLIC TELLURIDES
WITTIG-HORNER REACTION
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:11336/128126

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network_name_str CONICET Digital (CONICET)
spelling Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]tellurideSilveira, Claudio C.Rinaldi, FrancieliBassaco, Mariana M.Kaufman, Teodoro Saul3,4-DIHYDRO-2H-TELLUROPYRANSTANDEM REACTIONSVINYLIC TELLURIDESWITTIG-HORNER REACTIONhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The NaH-promoted tandem Michael addition/intramolecular Wittig-Horner reaction of bis[(diphenylphosphinoyl) methyl]telluride with chalcones stereoselectively afforded trans-2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro- 2H-telluropyran derivatives in 51-72% yield, under mild conditions.Fil: Silveira, Claudio C.. Universidade Federal de Santa Maria; BrasilFil: Rinaldi, Francieli. Universidade Federal de Santa Maria; BrasilFil: Bassaco, Mariana M.. Universidade Federal de Santa Maria; BrasilFil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; ArgentinaPergamon-Elsevier Science Ltd2010-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/128126Silveira, Claudio C.; Rinaldi, Francieli; Bassaco, Mariana M.; Kaufman, Teodoro Saul; Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 51; 34; 8-2010; 4563-45650040-4039CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0040403910011287info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2010.06.113info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:09:33Zoai:ri.conicet.gov.ar:11336/128126instacron: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 10:09:33.544CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
title Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
spellingShingle Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
Silveira, Claudio C.
3,4-DIHYDRO-2H-TELLUROPYRANS
TANDEM REACTIONS
VINYLIC TELLURIDES
WITTIG-HORNER REACTION
title_short Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
title_full Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
title_fullStr Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
title_full_unstemmed Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
title_sort Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride
dc.creator.none.fl_str_mv Silveira, Claudio C.
Rinaldi, Francieli
Bassaco, Mariana M.
Kaufman, Teodoro Saul
author Silveira, Claudio C.
author_facet Silveira, Claudio C.
Rinaldi, Francieli
Bassaco, Mariana M.
Kaufman, Teodoro Saul
author_role author
author2 Rinaldi, Francieli
Bassaco, Mariana M.
Kaufman, Teodoro Saul
author2_role author
author
author
dc.subject.none.fl_str_mv 3,4-DIHYDRO-2H-TELLUROPYRANS
TANDEM REACTIONS
VINYLIC TELLURIDES
WITTIG-HORNER REACTION
topic 3,4-DIHYDRO-2H-TELLUROPYRANS
TANDEM REACTIONS
VINYLIC TELLURIDES
WITTIG-HORNER REACTION
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 NaH-promoted tandem Michael addition/intramolecular Wittig-Horner reaction of bis[(diphenylphosphinoyl) methyl]telluride with chalcones stereoselectively afforded trans-2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro- 2H-telluropyran derivatives in 51-72% yield, under mild conditions.
Fil: Silveira, Claudio C.. Universidade Federal de Santa Maria; Brasil
Fil: Rinaldi, Francieli. Universidade Federal de Santa Maria; Brasil
Fil: Bassaco, Mariana M.. Universidade Federal de Santa Maria; Brasil
Fil: Kaufman, Teodoro Saul. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Química Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario; Argentina
description The NaH-promoted tandem Michael addition/intramolecular Wittig-Horner reaction of bis[(diphenylphosphinoyl) methyl]telluride with chalcones stereoselectively afforded trans-2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro- 2H-telluropyran derivatives in 51-72% yield, under mild conditions.
publishDate 2010
dc.date.none.fl_str_mv 2010-08
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/11336/128126
Silveira, Claudio C.; Rinaldi, Francieli; Bassaco, Mariana M.; Kaufman, Teodoro Saul; Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 51; 34; 8-2010; 4563-4565
0040-4039
CONICET Digital
CONICET
url http://hdl.handle.net/11336/128126
identifier_str_mv Silveira, Claudio C.; Rinaldi, Francieli; Bassaco, Mariana M.; Kaufman, Teodoro Saul; Synthesis of 2-diphenylphosphinoyl-3,5-diaryl-3,4-dihydro-2H-telluropyrans by reaction of chalcones with bis[(diphenylphosphinoyl)methyl]telluride; Pergamon-Elsevier Science Ltd; Tetrahedron Letters; 51; 34; 8-2010; 4563-4565
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/url/https://www.sciencedirect.com/science/article/abs/pii/S0040403910011287
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.tetlet.2010.06.113
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 Pergamon-Elsevier Science Ltd
publisher.none.fl_str_mv Pergamon-Elsevier Science Ltd
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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