Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners

Autores
Pergomet, Jorgelina Leonor; Kaufman, Teodoro Saúl; Bracca, Andrea Beatriz Juana
Año de publicación
2016
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil: Fil: Pergomet, Jorgelina Leonor. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Kaufman, Teodoro Saúl. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Bracca, Andrea Beatriz Juana. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Materia
6-Bromo-2-isopropylidenecoumaranone
TMC-120B
Pseudodeflectusin
Natural Product Synthesis
Prolinemediated Cyclization
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
RepHipUNR (UNR)
Institución
Universidad Nacional de Rosario
OAI Identificador
oai:rephip.unr.edu.ar:2133/10498
Acceder
id RepHipUNR_299ef4dd3aa088914c87c47c01148d08
oai_identifier_str oai:rephip.unr.edu.ar:2133/10498
network_acronym_str RepHipUNR
repository_id_str 1550
network_name_str RepHipUNR (UNR)
spelling Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congenersPergomet, Jorgelina LeonorKaufman, Teodoro SaúlBracca, Andrea Beatriz Juana6-Bromo-2-isopropylidenecoumaranoneTMC-120BPseudodeflectusinNatural Product SynthesisProlinemediated CyclizationFil: Fil: Pergomet, Jorgelina Leonor. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.Fil: Fil: Kaufman, Teodoro Saúl. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.Fil: Fil: Bracca, Andrea Beatriz Juana. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.Wiley2016-05-17info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/2133/10498urn:issn: 0018-019Xenghttp://onlinelibrary.wiley.com/doi/10.1002/hlca.201500525/abstracthttp://dx.doi.org/doi:10.1002/hlca.201500525info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/2.5/ar/Licencia RepHipreponame:RepHipUNR (UNR)instname:Universidad Nacional de Rosario2025-09-29T13:40:44Zoai:rephip.unr.edu.ar:2133/10498instacron:UNRInstitucionalhttps://rephip.unr.edu.ar/Universidad públicaNo correspondehttps://rephip.unr.edu.ar/oai/requestrephip@unr.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:15502025-09-29 13:40:44.508RepHipUNR (UNR) - Universidad Nacional de Rosariofalse
dc.title.none.fl_str_mv Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
title Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
spellingShingle Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
Pergomet, Jorgelina Leonor
6-Bromo-2-isopropylidenecoumaranone
TMC-120B
Pseudodeflectusin
Natural Product Synthesis
Prolinemediated Cyclization
title_short Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
title_full Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
title_fullStr Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
title_full_unstemmed Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
title_sort Expedient approach to 6-bromo-2-isopropylidenecoumaranone, a potential intermediate for the synthesis of TMC-120B, pseudodeflectusin, and Their congeners
dc.creator.none.fl_str_mv Pergomet, Jorgelina Leonor
Kaufman, Teodoro Saúl
Bracca, Andrea Beatriz Juana
author Pergomet, Jorgelina Leonor
author_facet Pergomet, Jorgelina Leonor
Kaufman, Teodoro Saúl
Bracca, Andrea Beatriz Juana
author_role author
author2 Kaufman, Teodoro Saúl
Bracca, Andrea Beatriz Juana
author2_role author
author
dc.subject.none.fl_str_mv 6-Bromo-2-isopropylidenecoumaranone
TMC-120B
Pseudodeflectusin
Natural Product Synthesis
Prolinemediated Cyclization
topic 6-Bromo-2-isopropylidenecoumaranone
TMC-120B
Pseudodeflectusin
Natural Product Synthesis
Prolinemediated Cyclization
dc.description.none.fl_txt_mv Fil: Fil: Pergomet, Jorgelina Leonor. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Kaufman, Teodoro Saúl. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Bracca, Andrea Beatriz Juana. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
description Fil: Fil: Pergomet, Jorgelina Leonor. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
publishDate 2016
dc.date.none.fl_str_mv 2016-05-17
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/2133/10498
urn:issn: 0018-019X
url http://hdl.handle.net/2133/10498
identifier_str_mv urn:issn: 0018-019X
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://onlinelibrary.wiley.com/doi/10.1002/hlca.201500525/abstract
http://dx.doi.org/doi:10.1002/hlca.201500525
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Licencia RepHip
eu_rights_str_mv openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Licencia RepHip
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Wiley
publisher.none.fl_str_mv Wiley
dc.source.none.fl_str_mv reponame:RepHipUNR (UNR)
instname:Universidad Nacional de Rosario
reponame_str RepHipUNR (UNR)
collection RepHipUNR (UNR)
instname_str Universidad Nacional de Rosario
repository.name.fl_str_mv RepHipUNR (UNR) - Universidad Nacional de Rosario
repository.mail.fl_str_mv rephip@unr.edu.ar
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