An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes

Autores
La Venia, Agustina; Dzijak, Rastislav; Rampmaier, Robert; Vrabel, Milan
Año de publicación
2021
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Fil: Fil: La Venia, Agustina. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: La Venia, Agustina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Dzijak, Rastislav. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: Rampmaier, Robert. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: Vrabel, Milan. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Materia
Bioorthogonal reactions
Click chemistry
Peptides
Solid-phase synthesis
Strained dienophiles
Nivel de accesibilidad
acceso abierto
Condiciones de uso
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Repositorio
RepHipUNR (UNR)
Institución
Universidad Nacional de Rosario
OAI Identificador
oai:rephip.unr.edu.ar:2133/23309
Acceder
id RepHipUNR_644195f10bdcc11f80ccd097ad30ac81
oai_identifier_str oai:rephip.unr.edu.ar:2133/23309
network_acronym_str RepHipUNR
repository_id_str 1550
network_name_str RepHipUNR (UNR)
spelling An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probesLa Venia, AgustinaDzijak, RastislavRampmaier, RobertVrabel, MilanBioorthogonal reactionsClick chemistryPeptidesSolid-phase synthesisStrained dienophilesFil: Fil: La Venia, Agustina. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.Fil: Fil: La Venia, Agustina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.Fil: Fil: Dzijak, Rastislav. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.Fil: Fil: Rampmaier, Robert. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.Fil: Fil: Vrabel, Milan. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.John Wiley and Sons Inc2021-09-24info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://hdl.handle.net/2133/23309urn:issn: 1521-3765enghttps://doi.org/10.1002/chem.202102042https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202102042info:eu-repo/semantics/openAccessAttribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)Licencia RepHipreponame:RepHipUNR (UNR)instname:Universidad Nacional de Rosario2025-09-29T13:41:49Zoai:rephip.unr.edu.ar:2133/23309instacron:UNRInstitucionalhttps://rephip.unr.edu.ar/Universidad públicaNo correspondehttps://rephip.unr.edu.ar/oai/requestrephip@unr.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:15502025-09-29 13:41:49.482RepHipUNR (UNR) - Universidad Nacional de Rosariofalse
dc.title.none.fl_str_mv An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
title An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
spellingShingle An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
La Venia, Agustina
Bioorthogonal reactions
Click chemistry
Peptides
Solid-phase synthesis
Strained dienophiles
title_short An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
title_full An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
title_fullStr An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
title_full_unstemmed An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
title_sort An optimized protocol for the synthesis of peptides Containing trans-Cyclooctene and Bicyclononyne Dienophiles as useful multifunctional bioorthogonal probes
dc.creator.none.fl_str_mv La Venia, Agustina
Dzijak, Rastislav
Rampmaier, Robert
Vrabel, Milan
author La Venia, Agustina
author_facet La Venia, Agustina
Dzijak, Rastislav
Rampmaier, Robert
Vrabel, Milan
author_role author
author2 Dzijak, Rastislav
Rampmaier, Robert
Vrabel, Milan
author2_role author
author
author
dc.subject.none.fl_str_mv Bioorthogonal reactions
Click chemistry
Peptides
Solid-phase synthesis
Strained dienophiles
topic Bioorthogonal reactions
Click chemistry
Peptides
Solid-phase synthesis
Strained dienophiles
dc.description.none.fl_txt_mv Fil: Fil: La Venia, Agustina. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: La Venia, Agustina. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Química Rosario (IQUIR-CONICET); Argentina.
Fil: Fil: Dzijak, Rastislav. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: Rampmaier, Robert. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
Fil: Fil: Vrabel, Milan. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
description Fil: Fil: La Venia, Agustina. Czech Academy of Sciences. Institute of Organic Chemistry and Biochemistry; Czech Republic.
publishDate 2021
dc.date.none.fl_str_mv 2021-09-24
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/2133/23309
urn:issn: 1521-3765
url http://hdl.handle.net/2133/23309
identifier_str_mv urn:issn: 1521-3765
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://doi.org/10.1002/chem.202102042
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202102042
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Licencia RepHip
eu_rights_str_mv openAccess
rights_invalid_str_mv Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
Licencia RepHip
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv John Wiley and Sons Inc
publisher.none.fl_str_mv John Wiley and Sons Inc
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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score 13.070432

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