Por favor, use este identificador para citar o enlazar a este item:
http://hdl.handle.net/10261/271804
COMPARTIR / EXPORTAR:
SHARE CORE BASE | |
Visualizar otros formatos: MARC | Dublin Core | RDF | ORE | MODS | METS | DIDL | DATACITE | |
Campo DC | Valor | Lengua/Idioma |
---|---|---|
dc.contributor.author | Ardevines, Sandra | es_ES |
dc.contributor.author | Marqués-López, Eugenia | es_ES |
dc.contributor.author | Herrera, Raquel P. | es_ES |
dc.date.accessioned | 2022-06-07T12:27:30Z | - |
dc.date.available | 2022-06-07T12:27:30Z | - |
dc.date.issued | 2022 | - |
dc.identifier.citation | Catalysts 12(1): 101 (2022) | es_ES |
dc.identifier.uri | http://hdl.handle.net/10261/271804 | - |
dc.description.abstract | Nowadays, the development of new enantioselective processes is highly relevant in chemistry due to the relevance of chiral compounds in biomedicine (mainly drugs) and in other fields, such as agrochemistry, animal feed, and flavorings. Among them, organocatalytic methods have become an efficient and sustainable alternative since List and MacMillan pioneering contributions were published in 2000. These works established the term asymmetric organocatalysis to label this area of research, which has grown exponentially over the last two decades. Since then, the scientific community has attended to the discovery of a plethora of organic reactions and transformations carried out with excellent results in terms of both reactivity and enantioselectivity. Looking back to earlier times, we can find in the literature a few examples where small organic molecules and some natural products could act as effective catalysts. However, with the birth of this type of catalysis, new chemical architectures based on amines, thioureas, squaramides, cinchona alkaloids, quaternary ammonium salts, carbenes, guanidines and phosphoric acids, among many others, have been developed. These organocatalysts have provided a broad range of activation modes that allow privileged interactions between catalysts and substrates for the preparation of compounds with high added value in an enantioselective way. Here, we briefly cover the history of this chemistry, from our point of view, including our beginnings, how the field has evolved during these years of research, and the road ahead. | es_ES |
dc.description.sponsorship | This research was funded by Agencia Estatal de Investigación (AEI), project PID2020-117455GB-I00/AEI/10.13039/501100011033; and Gobierno de Aragón-Fondo Social Europeo (Research Group E07_20R). | es_ES |
dc.language.iso | eng | es_ES |
dc.publisher | Multidisciplinary Digital Publishing Institute | es_ES |
dc.relation | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2020-117455GB-I00/ES/CATALISIS MULTIFUNCIONAL PARA LA CONSTRUCCION DE COMPLEJIDAD MOLECULAR. ESTUDIO DE SUS PROPIEDADES Y APLICACIONES / | es_ES |
dc.relation.isversionof | Publisher's version | es_ES |
dc.rights | openAccess | es_ES |
dc.subject | Chirality | es_ES |
dc.subject | Sustainability | es_ES |
dc.subject | Enantioselective | es_ES |
dc.subject | Organocatalysis | es_ES |
dc.subject | Green chemistry | es_ES |
dc.title | Horizons in asymmetric organocatalysis: En Route to the sustainability and new applications | es_ES |
dc.type | artículo | es_ES |
dc.identifier.doi | 10.3390/catal12010101 | - |
dc.description.peerreviewed | Peer reviewed | es_ES |
dc.relation.publisherversion | https://doi.org/10.3390/catal12010101 | es_ES |
dc.identifier.e-issn | 2073-4344 | - |
dc.rights.license | https://creativecommons.org/licenses/by/4.0/ | es_ES |
dc.contributor.funder | Ministerio de Ciencia, Innovación y Universidades (España) | es_ES |
dc.contributor.funder | Agencia Estatal de Investigación (España) | es_ES |
dc.contributor.funder | Gobierno de Aragón | es_ES |
dc.contributor.funder | European Commission | es_ES |
dc.relation.csic | Sí | es_ES |
oprm.item.hasRevision | no ko 0 false | * |
dc.identifier.funder | http://dx.doi.org/10.13039/501100010067 | es_ES |
dc.identifier.funder | http://dx.doi.org/10.13039/501100011033 | es_ES |
dc.identifier.funder | http://dx.doi.org/10.13039/501100000780 | es_ES |
dc.type.coar | http://purl.org/coar/resource_type/c_6501 | es_ES |
item.grantfulltext | open | - |
item.fulltext | With Fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairetype | artículo | - |
Aparece en las colecciones: | (ISQCH) Artículos |
Ficheros en este ítem:
Fichero | Descripción | Tamaño | Formato | |
---|---|---|---|---|
horizonappli.pdf | 3,78 MB | Adobe PDF | Visualizar/Abrir |
CORE Recommender
SCOPUSTM
Citations
12
checked on 11-may-2024
WEB OF SCIENCETM
Citations
8
checked on 29-feb-2024
Page view(s)
39
checked on 21-may-2024
Download(s)
36
checked on 21-may-2024
Google ScholarTM
Check
Altmetric
Altmetric
Este item está licenciado bajo una Licencia Creative Commons