Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling
The preparation of complex architectures has inspired the search for new methods and new processes in organic synthesis. Multicomponent reactions have become an interesting approach to achieve such molecular diversity and complexity. This review intends to illustrate important gold-catalyzed example...
- Autores:
-
Visbal Acevedo, Renso Raul
Graus, Sara
Herrera Perez, Raquel
Gimeno M, Concepción
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2018
- Institución:
- Corporación Universidad de la Costa
- Repositorio:
- REDICUC - Repositorio CUC
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.cuc.edu.co:11323/1032
- Acceso en línea:
- https://hdl.handle.net/11323/1032
https://repositorio.cuc.edu.co/
- Palabra clave:
- 4-Dihydropyridines
Multicomponent Reactions
Oxazoles
Pyridines
Spirocycle
Thiazolo-Quinolines
4-Dihydropyrimidin-2(1H)-Ones; 1
Β-Alkoxyketones
Butenolides
Catalysis
Ethers
Gold; 3
- Rights
- openAccess
- License
- Atribución – No comercial – Compartir igual
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|
dc.title.eng.fl_str_mv |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
title |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
spellingShingle |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling 4-Dihydropyridines Multicomponent Reactions Oxazoles Pyridines Spirocycle Thiazolo-Quinolines 4-Dihydropyrimidin-2(1H)-Ones; 1 Β-Alkoxyketones Butenolides Catalysis Ethers Gold; 3 |
title_short |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
title_full |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
title_fullStr |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
title_full_unstemmed |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
title_sort |
Gold Catalyzed Multicomponent Reactions Beyond A3 Coupling |
dc.creator.fl_str_mv |
Visbal Acevedo, Renso Raul Graus, Sara Herrera Perez, Raquel Gimeno M, Concepción |
dc.contributor.author.spa.fl_str_mv |
Visbal Acevedo, Renso Raul Graus, Sara Herrera Perez, Raquel Gimeno M, Concepción |
dc.subject.eng.fl_str_mv |
4-Dihydropyridines Multicomponent Reactions Oxazoles Pyridines Spirocycle Thiazolo-Quinolines 4-Dihydropyrimidin-2(1H)-Ones; 1 Β-Alkoxyketones Butenolides Catalysis Ethers Gold; 3 |
topic |
4-Dihydropyridines Multicomponent Reactions Oxazoles Pyridines Spirocycle Thiazolo-Quinolines 4-Dihydropyrimidin-2(1H)-Ones; 1 Β-Alkoxyketones Butenolides Catalysis Ethers Gold; 3 |
description |
The preparation of complex architectures has inspired the search for new methods and new processes in organic synthesis. Multicomponent reactions have become an interesting approach to achieve such molecular diversity and complexity. This review intends to illustrate important gold-catalyzed examples for the past ten years leading to interesting skeletons involved in biologically active compounds. |
publishDate |
2018 |
dc.date.accessioned.none.fl_str_mv |
2018-11-15T16:28:39Z |
dc.date.available.none.fl_str_mv |
2018-11-15T16:28:39Z |
dc.date.issued.none.fl_str_mv |
2018-09-04 |
dc.type.spa.fl_str_mv |
Artículo de revista |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.content.spa.fl_str_mv |
Text |
dc.type.driver.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.redcol.spa.fl_str_mv |
http://purl.org/redcol/resource_type/ART |
dc.type.version.spa.fl_str_mv |
info:eu-repo/semantics/acceptedVersion |
format |
http://purl.org/coar/resource_type/c_6501 |
status_str |
acceptedVersion |
dc.identifier.issn.spa.fl_str_mv |
14203049 |
dc.identifier.uri.spa.fl_str_mv |
https://hdl.handle.net/11323/1032 |
dc.identifier.instname.spa.fl_str_mv |
Corporación Universidad de la Costa |
dc.identifier.reponame.spa.fl_str_mv |
REDICUC - Repositorio CUC |
dc.identifier.repourl.spa.fl_str_mv |
https://repositorio.cuc.edu.co/ |
identifier_str_mv |
14203049 Corporación Universidad de la Costa REDICUC - Repositorio CUC |
url |
https://hdl.handle.net/11323/1032 https://repositorio.cuc.edu.co/ |
dc.language.iso.none.fl_str_mv |
eng |
language |
eng |
dc.rights.spa.fl_str_mv |
Atribución – No comercial – Compartir igual |
dc.rights.accessrights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
rights_invalid_str_mv |
Atribución – No comercial – Compartir igual http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
institution |
Corporación Universidad de la Costa |
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Visbal Acevedo, Renso RaulGraus, SaraHerrera Perez, RaquelGimeno M, Concepción2018-11-15T16:28:39Z2018-11-15T16:28:39Z2018-09-0414203049https://hdl.handle.net/11323/1032Corporación Universidad de la CostaREDICUC - Repositorio CUChttps://repositorio.cuc.edu.co/The preparation of complex architectures has inspired the search for new methods and new processes in organic synthesis. Multicomponent reactions have become an interesting approach to achieve such molecular diversity and complexity. This review intends to illustrate important gold-catalyzed examples for the past ten years leading to interesting skeletons involved in biologically active compounds.Visbal Acevedo, Renso Raul-9ef96ca4-74a6-4585-bf26-5288033eec5b-600Graus, Sara-f809bc70-88e9-4711-8229-24b8a886ef33-600Herrera Perez, Raquel-9f64f685-57ad-4c58-9613-f26353ce7eb3-600Gimeno M, Concepción-cdd45bec-d463-4916-8658-b092ce2f150e-600engAtribución – No comercial – Compartir igualinfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf24-DihydropyridinesMulticomponent ReactionsOxazolesPyridinesSpirocycleThiazolo-Quinolines4-Dihydropyrimidin-2(1H)-Ones; 1Β-AlkoxyketonesButenolidesCatalysisEthersGold; 3Gold Catalyzed Multicomponent Reactions Beyond A3 CouplingArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Textinfo:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTinfo:eu-repo/semantics/acceptedVersionPublicationORIGINALGold catalyzed multicomponent.pdfGold catalyzed multicomponent.pdfapplication/pdf6761260https://repositorio.cuc.edu.co/bitstreams/8054f9ec-e3db-4df4-a15d-7982a0c3cf21/downloadcfd909bb775bc8df1399f0083d361547MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.cuc.edu.co/bitstreams/73ff5222-2a6b-49f5-b17b-f95ff5984aac/download8a4605be74aa9ea9d79846c1fba20a33MD52THUMBNAILGold catalyzed multicomponent.pdf.jpgGold catalyzed multicomponent.pdf.jpgimage/jpeg67067https://repositorio.cuc.edu.co/bitstreams/f33259c5-baf0-4c88-9207-d2de0dc726d5/downloadde539e118154045992da7094713ba142MD54TEXTGold catalyzed multicomponent.pdf.txtGold catalyzed multicomponent.pdf.txttext/plain86925https://repositorio.cuc.edu.co/bitstreams/3117514f-3def-415c-baed-c91b48a6744c/downloaddedcb9c140055f1ef8690fb5f23b47cdMD5511323/1032oai:repositorio.cuc.edu.co:11323/10322024-09-17 12:49:48.746open.accesshttps://repositorio.cuc.edu.coRepositorio de la Universidad de la Costa CUCrepdigital@cuc.edu.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 |