Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry

The synthesis of a new highly symmetric hexakis adduct of C60 appended with 12 cyclooctyne moieties has been carried out. This compound has been used for the copper-free strain-promoted cycloaddition reaction to a series of azides with excellent yields.This strategy for the obtention of clicked addu...

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Detalles Bibliográficos
Autores: Ramos, Soriano, Reina, José J., Pérez, Sánchez, Illescas, Beatriz M., Rojo, Javier, Martín, Nazario
Tipo de recurso: artículo
Fecha de publicación:2016
País:España
Institución:Universidad Complutense de Madrid (UCM)
Repositorio:Docta Complutense
Idioma:inglés
OAI Identifier:oai:docta.ucm.es:20.500.14352/23178
Acceso en línea:https://hdl.handle.net/20.500.14352/23178
Access Level:acceso abierto
Palabra clave:547
Química orgánica (Química)
2306 Química Orgánica
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spelling Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistryRamos, SorianoReina, José J.Pérez, SánchezIllescas, Beatriz M.Rojo, JavierMartín, Nazario547Química orgánica (Química)2306 Química OrgánicaThe synthesis of a new highly symmetric hexakis adduct of C60 appended with 12 cyclooctyne moieties has been carried out. This compound has been used for the copper-free strain-promoted cycloaddition reaction to a series of azides with excellent yields.This strategy for the obtention of clicked adducts of [60]fullerene is of special interest for biological applications.RSCUniversidad Complutense de Madrid20162016-07-0120162016-07-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/20.500.14352/23178reponame:Docta Complutenseinstname:Universidad Complutense de Madrid (UCM)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:docta.ucm.es:20.500.14352/231782026-06-02T12:44:21Z
dc.title.none.fl_str_mv Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
title Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
spellingShingle Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
Ramos, Soriano
547
Química orgánica (Química)
2306 Química Orgánica
title_short Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
title_full Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
title_fullStr Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
title_full_unstemmed Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
title_sort Cyclooctyne [60]fullerene hexakis adducts: a globular scaffold for copper-free click chemistry
dc.creator.none.fl_str_mv Ramos, Soriano
Reina, José J.
Pérez, Sánchez
Illescas, Beatriz M.
Rojo, Javier
Martín, Nazario
author Ramos, Soriano
author_facet Ramos, Soriano
Reina, José J.
Pérez, Sánchez
Illescas, Beatriz M.
Rojo, Javier
Martín, Nazario
author_role author
author2 Reina, José J.
Pérez, Sánchez
Illescas, Beatriz M.
Rojo, Javier
Martín, Nazario
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidad Complutense de Madrid
dc.subject.none.fl_str_mv 547
Química orgánica (Química)
2306 Química Orgánica
topic 547
Química orgánica (Química)
2306 Química Orgánica
description The synthesis of a new highly symmetric hexakis adduct of C60 appended with 12 cyclooctyne moieties has been carried out. This compound has been used for the copper-free strain-promoted cycloaddition reaction to a series of azides with excellent yields.This strategy for the obtention of clicked adducts of [60]fullerene is of special interest for biological applications.
publishDate 2016
dc.date.none.fl_str_mv 2016
2016-07-01
2016
2016-07-01
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/20.500.14352/23178
url https://hdl.handle.net/20.500.14352/23178
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv RSC
publisher.none.fl_str_mv RSC
dc.source.none.fl_str_mv reponame:Docta Complutense
instname:Universidad Complutense de Madrid (UCM)
instname_str Universidad Complutense de Madrid (UCM)
reponame_str Docta Complutense
collection Docta Complutense
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15.300724

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